Reaxys
PubChem
eMolecules
Reactions (272)
Yield
Substances (3)
Citations (326)
Conditions
References A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
100
Synthesize Find similar Rx-ID: 6730721 Find similar reactions
With oxygen; phosphorus trichoride
T=-10 - 10°C; Title compound not separated from byproducts;
Dogadina, A. V.; Efanov, V. A.; Belykh, O. A.; Komarov, V. Ya.; Ionin, B. I.; Petrov, A. A.
J. Gen. Chem. USSR (Engl. Transl.), 1984 , vol. 54, # 4 p. 796 - 804,706 - 713 Title/Abstract Full Text Show Details
With oxygen; phosphorus trichoride
T=-10 - 10°C; Product distributionMechanism;
Dogadina, A. V.; Efanov, V. A.; Belykh, O. A.; Komarov, V. Ya.; Ionin, B. I.; Petrov, A. A.
J. Gen. Chem. USSR (Engl. Transl.), 1984 , vol. 54, # 4 p. 796 - 804,706 - 713 Title/Abstract Full Text Show Details
A
B
101
Synthesize Find similar Rx-ID: 8287157 Find similar reactions
Synthesize Find similar
Synthesize Find similar
With sulfuryl dichloride
T=18 - 31°C; 5.83333 h; Product distribution;
Nakamura, Shigeaki
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1983 , p. 1 - 4 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
102
Synthesize Find similar Rx-ID: 8287158 Find similar reactions
With sulfuryl dichloride
T=18 - 31°C; 0.333333 h; Product distribution;
Nakamura, Shigeaki
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1983 , p. 1 - 4 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
103
Synthesize Find similar Rx-ID: 8287159 Find similar reactions
With sulfuryl dichloride
T=18 - 31°C; 0.5 h; Product distribution;
Nakamura, Shigeaki
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1983 , p. 1 - 4 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
104
Synthesize Find similar
Synthesize Find similar
Rx-ID: 1757306 Find similar reactions
Mirek, Julian; Haas, Alois
Journal of Fluorine Chemistry, 1982 , vol. 19, p. 67 - 70 Title/Abstract Full Text View citing articles Show Details
in diethyl ether
Ambient temperature; Yield given;
A
B
Synthesize Find similar
Synthesize Find similar
105
Synthesize Find similar
Synthesize Find similar
Rx-ID: 1963516 Find similar reactions
Mirek, Julian; Haas, Alois
Journal of Fluorine Chemistry, 1982 , vol. 19, p. 67 - 70 Title/Abstract Full Text View citing articles Show Details
in diethyl ether
Ambient temperature; Yield given;
A
B
C
D
E
F
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
106
Synthesize Find similar Rx-ID: 2842707 Find similar reactions
A: 20 % Spectr. C: 20 % Spectr. D: 72 %
With tetrachloromethane
T=79.5°C; 72 h; other oxadiazoline; Rate constantMechanismProduct distribution;
Bekhazi, Michel; Warkentin, John
Journal of Organic Chemistry, 1982 , vol. 47, # 25 p. 4870 - 4873 Title/Abstract Full Text View citing articles Show Details
Spectr. E: 9 % Spectr. F: 50 % Spectr. A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
107
Synthesize Find similar Rx-ID: 2842708 Find similar reactions
B: 20 % Spectr. C: 72 % Spectr. D: 50 % Spectr.
With tetrachloromethane
T=79.5°C; 72 h; Further byproducts given;
Bekhazi, Michel; Warkentin, John
Journal of Organic Chemistry, 1982 , vol. 47, # 25 p. 4870 - 4873 Title/Abstract Full Text View citing articles Show Details
B: 20 % Spectr. C: 72 % Spectr. D: 50 % Spectr.
in tetrachloromethane
T=79.5°C; 72 h; Further byproducts given;
Bekhazi, Michel; Warkentin, John
Journal of Organic Chemistry, 1982 , vol. 47, # 25 p. 4870 - 4873 Title/Abstract Full Text View citing articles Show Details
108
Synthesize Find similar
109
With sulfuryl dichloride; triphenylphosphine
Yield given. Multistep reaction;
Synthesize Find similar
Rx-ID: 3784368 Find similar reactions
Still, Ian W. J.; Kutney, Gerald W.; McLean, David
Journal of Organic Chemistry, 1982 , vol. 47, # 3 p. 560 - 561 Title/Abstract Full Text View citing articles Show Details
Synthesize Find similar
Synthesize Find similar
Rx-ID: 572566 Find similar reactions
95%
With phosphorus trichoride
T=20°C; 16 h;
Michie, Jacqui K.; Miller, Allen J.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981 , p. 785 - 788 Title/Abstract Full Text View citing articles Show Details
With hydrogenchloride
Nametkin; Brjussowa; Fedossejewa
Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1939 , vol. 12, p. 1698 Chem.Abstr., 1940 , p. 7283 Full Text Show Details
With thionyl chloride
T=20 - 25°C;
Elko Chem.Co.
Patent: US1819613 , 1928 ; Full Text Show Details
Hide Details
With phosphorus pentachloride
de Pascual Teresa; Garrido Espinosa
Anales de la Real Sociedad Espanola de Fisica y Quimica, Serie B: Quimica, 1956 , vol. 52, p. 447,456 Full Text View citing articles Show Details
With calcium chloride
Gmuender
Helvetica Chimica Acta, 1953 , vol. 36, p. 2021 Full Text Show Details
With chlorine
Gal
Annales de Chimie (Cachan, France), 1862 , vol. <3>66, p. 188,190 Full Text Show Details
With hydrogenchloride
Gal
Annales de Chimie (Cachan, France), 1862 , vol. <3>66, p. 188,190 Full Text Show Details
With phosphorus pentachloride
Ritter
Justus Liebigs Annalen der Chemie, 1855 , vol. 95, p. 208 Full Text Show Details
With phosphorus trichoride
Bechamp
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1855 , vol. 40, p. 946 Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1856 , vol. 42, p. 226 Full Text Show Details
A
B
110
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2075085 Find similar reactions
Synthesize Find similar
With phosphorus trichoride
T=20°C; 2 h; Title compound not separated from byproducts;
Michie, Jacqui K.; Miller, Allen J.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981 , p. 785 - 788 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
111
Synthesize Find similar
Synthesize Find similar
Rx-ID: 2360041 Find similar reactions
A: 89%
With phosphorus trichoride in chloroform-d1
T=20°C; 16 h;
Michie, Jacqui K.; Miller, Allen J.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981 , p. 785 - 788 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
112
Synthesize Find similar Rx-ID: 2391555 Find similar reactions
With phosphorus trichoride
T=20°C; 16 h; Title compound not separated from byproducts;
Michie, Jacqui K.; Miller, Allen J.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981 , p. 785 - 788 Title/Abstract Full Text View citing articles Show Details
113
Synthesize Find similar
84 % Spectr.
Synthesize Find similar
Rx-ID: 1853288 Find similar reactions
With pyridine; tributyltin chloride
T=40°C; Δ G; Thermodynamic dataEquilibrium constant;
Friedrich, Edwin C.; Abma, Charles B.
Journal of the American Chemical Society, 1980 , vol. 102, # 4 p. 1367 - 1371 Title/Abstract Full Text View citing articles Show Details
114
Synthesize Find similar
92 % Spectr.
Synthesize Find similar
Rx-ID: 1916615 Find similar reactions
With pyridine; tributyltin chloride
T=40°C; Δ G; Thermodynamic dataEquilibrium constant;
Friedrich, Edwin C.; Abma, Charles B.
Journal of the American Chemical Society, 1980 , vol. 102, # 4 p. 1367 - 1371 Title/Abstract Full Text View citing articles Show Details
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
115
Synthesize Find similar Rx-ID: 3354584 Find similar reactions
Synthesize Find similar
Broomhead, Eleanor J.; McLauchlan, Keith A.; Roe, Jonathan C.
Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1980 , p. 796 - 804 Title/Abstract Full Text View citing articles Show Details
in various solvent(s) Irradiation; Product distribution;
A
B
C
D
E
F
116
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Rx-ID: 7452217 Find similar reactions
With perchloric acid in acetic acid
T=40°C; Product distributionKineticsMechanism;
Synthesize Find similar
Montheard; Camps; Ait-Yahia; Guilluy
Tetrahedron, 1980 , vol. 36, # 20-21 p. 2967 - 2975 Title/Abstract Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
117
Rx-ID: 25355212 Find similar reactions
BASF Aktiengesellschaft
Patent: US4203977 A1, 1980 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
5:EXAMPLE 5
EXAMPLE 5 Analogously to Example 4, there is obtained from 31.4 g of N,N-dimethylchloroacetamidine hydrochloride and 17.3 g of acetyl chloride 19 g of the compound STR10 as a yellowish oil; nD25: 1.5190. A
B
Synthesize Find similar
Synthesize Find similar
118
Hide Experimental Procedure
Synthesize Find similar
Rx-ID: 25283177 Find similar reactions
Diaz Chemical Corporation
Patent: US4163753 A1, 1979 ;
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Title/Abstract Full Text Show Details
2:EXAMPLE 2
EXAMPLE 2 To the reaction from example 1 without cleanout was added p-chlorobenzotrichloride (231 g, 1.0 mole), acetic anhydride (83.5 g, 0.82 mole) and sulfuric acid (1.0 g, 0.01 mole). The reaction was run similar to example 1. An additional 1.0 g of sulfuric acid was added after all of the acetyl chloride had been removed. The yield of acetyl chloride was 120 g (93.4percent) and the yield of p-chlorobenzoyl chloride was 176.3 g (100percent).
A: 136 g (91.2%)
Diaz Chemical Corporation
Patent: US4163753 A1, 1979 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
4:EXAMPLE 4
EXAMPLE 4 To the reaction residue from run 3 was added 230 g of p-chlorobenzotrichloride, 97 g of acetic anhydride and 2 g of sulfuric acid (98percent). The reaction was carried as previously described to give 136 g (91.2percent) of acetyl chloride and 177 g (101percent) of p-chlorobenzoyl chloride. The average yield from runs 1-4 was 92.7percent for acetyl chloride and 93percent for p-chlorobenzoyl chloride. A
B
Synthesize Find similar
Synthesize Find similar
119
Rx-ID: 25283178 Find similar reactions
Diaz Chemical Corporation
Patent: US4163753 A1, 1979 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
6:EXAMPLE 6
EXAMPLE 6 Benzotrichloride (195.5 g), acetic anhydride (98 g) and sulfuric acid were charged to the reactor. Acetyl chloride began to distill when the reaction mixture reached 118° C. The yield of acetyl chloride was 130 g (86.3percent) and the yield of benzoyl chloride was 130.9 g (93.1percent), b.p. 191°-193° C.
Diaz Chemical Corporation
Patent: US4163753 A1, 1979 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
9:EXAMPLE 9
EXAMPLE 9 In this run, the addition procedure was reversed with the benzotrichloride being added to the acetic anhydride and sulfuric acid over a 3 hour period. The yield of acetyl chloride was 145.59 (92.8percent) and the yield of benzoyl chloride was 102 gms (72.6percent). A
120
B
Synthesize Find similar
Synthesize Find similar
Rx-ID: 25283179 Find similar reactions
Hoechst Aktiengesellschaft
Patent: US4172845 A1, 1979 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
5:Preparation of 2-methyl-2,5-dioxo-1-oxa-2-phospholene- 3
Preparation of 2-methyl-2,5-dioxo-1-oxa-2-phospholene- 3 The [2-(chloroformyl)-vinyl]-methyl-phosphinic acid chloride prepared in the manner described in Example 1 was admixed dropwise at 70° C., over a period of 2.5 hours, with 548 g (5.37 mol) of acetic anhydride and the resulting acetyl chloride was distilled off through a column. A
B
Synthesize Find similar
Synthesize Find similar
121
Rx-ID: 25283180 Find similar reactions
Hoechst Aktiengesellschaft
Patent: US4172845 A1, 1979 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
6:Preparation of 2-phenyl-2,5-dioxo-1-oxa-2-phospholene-3.
Preparation of 2-phenyl-2,5-dioxo-1-oxa-2-phospholene-3. The [2-(chloroformyl)-vinyl]-phenyl-phosphinic acid chloride prepared in the manner described in Example 3 was admixed dropwise at 80°-85° C., within 45 minutes, with 230 g (2.25 mol) of acetic anhydride and the resulting acetyl chloride was distilled off through a column at 52° C. at atmospheric pressure. The residue was subjected to distillation under high vacuum. After an initial slight decomposition of the material in the flask accompanied by evolution of gas, there distilled over at 190°-195° C., under 0.6 mm Hg, 248 g of 2-phenyl-2,5-dioxo-1-oxa-2-phospholene-3 which was an oily liquid clear as water. The yield was 63.9percent of the theoretical, based on the phenyldichlorophosphane used. A
B
Synthesize
Synthesize
122
Synthesize Find similar
Rx-ID: 1017257 Find similar reactions
Find similar
Find similar
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
T=20°C; Equilibrium constant;
A
B
Synthesize Find similar
Synthesize Find similar
123
Synthesize Find similar Rx-ID: 1036891 Find similar reactions
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
T=20°C; Equilibrium constant;
A
B
Synthesize Find similar
Synthesize Find similar
124
Synthesize Find similar Rx-ID: 1037236 Find similar reactions
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
T=20°C; Equilibrium constant;
A
125
Synthesize
B
Find similar Rx-ID: 1037497 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
T=20°C; Equilibrium constant;
A
B
Synthesize Find similar
Synthesize Find similar
126
Synthesize Find similar Rx-ID: 1037525 Find similar reactions
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
T=20°C; Equilibrium constant;
A
B
Synthesize Find similar
Synthesize Find similar
127
Synthesize Find similar Rx-ID: 1060960 Find similar reactions
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
T=20°C; Equilibrium constant;
A
128
B
Synthesize Find similar Rx-ID: 1061594 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
T=20°C; Equilibrium constant;
A
B
Synthesize Find similar
Synthesize Find similar
129
Synthesize Find similar Rx-ID: 1072124 Find similar reactions
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
T=20°C; Equilibrium constant;
A
B
Synthesize Find similar
Synthesize Find similar
130
Synthesize Find similar Rx-ID: 1072455 Find similar reactions
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
T=20°C; Equilibrium constant;
A
131
B
Synthesize Find similar Rx-ID: 1073172 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
T=20°C; Equilibrium constant;
A
B
Synthesize Find similar
Synthesize Find similar
132
Synthesize Find similar Rx-ID: 1080725 Find similar reactions
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
in chloroform-d1
T=20°C; Equilibrium constant;
A
B
Synthesize Find similar
Synthesize Find similar
133
Synthesize Find similar Rx-ID: 1101115 Find similar reactions
With zinc(II) chloride in chloroform-d1
T=42°C; Equilibrium constant;
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
134
Synthesize Find similar Rx-ID: 1112456 Find similar reactions
With zinc(II) chloride in chloroform-d1
T=42°C; Equilibrium constant;
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
135
Synthesize Find similar Rx-ID: 1112725 Find similar reactions
With zinc(II) chloride in chloroform-d1
T=42°C; Equilibrium constant;
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
136
Synthesize Find similar Rx-ID: 1112726 Find similar reactions
With zinc(II) chloride in chloroform-d1
T=42°C; Equilibrium constant;
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
137
Synthesize Find similar Rx-ID: 1112727 Find similar reactions
With zinc(II) chloride in chloroform-d1
T=42°C; Equilibrium constant;
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
138
Synthesize Find similar Rx-ID: 1112975 Find similar reactions
With zinc(II) chloride in chloroform-d1
T=42°C; Equilibrium constant;
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
139
Synthesize Find similar Rx-ID: 1113937 Find similar reactions
With zinc(II) chloride in chloroform-d1
T=42°C; Equilibrium constant;
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
140
Synthesize Find similar Rx-ID: 1143464 Find similar reactions
With zinc(II) chloride in chloroform-d1
T=42°C; Equilibrium constant;
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
141
Synthesize Find similar Rx-ID: 1336329 Find similar reactions
With zinc(II) chloride in chloroform-d1
T=42°C; Equilibrium constant;
Bigler,P.; Neuenschwander,M.
Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
142
Hide Experimental Procedure
Rx-ID: 25210011 Find similar reactions
Schering Aktiengesellschaft
Patent: US3953501 A1, 1976 ; Title/Abstract Full Text Show Details
6:N-(3-Carboxy-5-acetamido-2,4,6-triiodobenzoyl)-β-alanine Methylamide
EXAMPLE 6 N-(3-Carboxy-5-acetamido-2,4,6-triiodobenzoyl)-β-alanine Methylamide 99.5 g. (0.15 mole) of N-(3-carboxy-5-amino-2,4,6-triiodobenzoyl)-β-alanine methylamide. 1.1 H2 O (IV f), m.p. 250°-252° C. (decomposition) in 190 ml. of dimethylacetamide yield, after reaction with 40.0 ml. of acetyl chloride analogously to Example 1, 60.4 g. (58.8percent) of the desired compound. A
B
Synthesize Find similar
Synthesize Find similar
143
Rx-ID: 25210012 Find similar reactions
Bayer Aktiengesellschaft
Patent: US3966964 A1, 1976 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
34:EXAMPLE 34
EXAMPLE 34 In analogy with Example 33 there is obtained from 3,5,3',4'-tetrachloro-thionosalicylic acid anilide and acetyl chloride, the compound 2-acetoxy-3,5-dichloro-N-(3',4'-dichlorophenyl)-thionobenzamide of m.p. 188°C. A
B
Synthesize Find similar
Synthesize Find similar
144
Rx-ID: 25210013 Find similar reactions
Bayer Aktiengesellschaft
Patent: US3966964 A1, 1976 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
70:EXAMPLE 70
EXAMPLE 70 Similarly to Example 33 there is obtained from 3,5-dichloro-3',5'-bis-trifluoromethyl-thionosalicylic acid anilide and acetylchloride the compound 2-acetoxy-3,5-dichloro-N-(3',5'-bis-trifluoromethyl-phenyl)-thionobenzamide. m.p. 129°C. A
145
B
Synthesize Find similar
Synthesize Find similar
Rx-ID: 25210014 Find similar reactions
Bayer Aktiengesellschaft
Patent: US3966964 A1, 1976 ;
Hide Experimental Procedure
Title/Abstract Full Text Show Details
76:EXAMPLE 76
EXAMPLE 76 Similarly to Example 33, there is obtained from 3,5,4'-trichloro-2'-methyl-thionosalicylic acid anilide and acetylchloride the compound 2-acetoxy-3,5-dichloro-N-(2'-methyl-4'-chlorophenyl)-thionobenzamide. m.p. 180°C. A
B
Synthesize Find similar
Synthesize Find similar
146
Synthesize Find similar
Synthesize Find similar
Rx-ID: 26619409 Find similar reactions
Blues et al.
Journal of the Chemical Society [Section] D: Chemical Communications, 1970 , p. 699 Full Text View citing articles Show Details
Gmelin Handbook: Ag: MVol.B5, 1.1.5, page 21 - 22 Full Text Show Details
in neat (no solvent) with excess HCl;;
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
147
Synthesize Find similar Rx-ID: 26619410 Find similar reactions
Synthesize Find similar
Blues et al.
Journal of the Chemical Society [Section] D: Chemical Communications, 1970 , p. 699 Full Text View citing articles Show Details
Gmelin Handbook: Ag: MVol.B5, 1.1.5, page 21 - 22 Full Text Show Details
in neat (no solvent) with gaseous HCl dild. with N2;;
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
148
Synthesize Find similar
Synthesize Find similar
Rx-ID: 26069147 Find similar reactions
Gmelin Handbook: Ni: MVol.B3, 44, page 865 - 867 Full Text Show Details
in neat (no solvent)
Khristov, D.; Karaivanov, S.; Kolushki, V.
Godishnik Sofiiskiya Univ. Fiz.-Mat. Fak. 3-Khim., 1960 , vol. 55, p. 49 - 66 C. A., 1963 , vol. 59, p. 3513 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
149
Synthesize Find similar Rx-ID: 7061156 Find similar reactions
Douglass
Journal of Organic Chemistry, 1959 , vol. 24, p. 2004 Full Text View citing articles Show Details
T=-10°C;
A
150
B
Synthesize Find similar Rx-ID: 124730 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Summerbell; Lunk
Journal of the American Chemical Society, 1958 , vol. 80, p. 604 Full Text View citing articles Show Details
T=190°C;
151
Synthesize Find similar
Rx-ID: 639367 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Heslinga et al.
Recueil des Travaux Chimiques des Pays-Bas, 1957 , vol. 76, p. 969,972 Full Text Show Details
152
Synthesize Find similar
Synthesize Find similar
Rx-ID: 254235 Find similar reactions
Gerrard; Wheelans
Journal of the Chemical Society, 1956 , p. 4296,4299 Full Text Show Details
T=150°C;
A
B
153
Synthesize Find similar Rx-ID: 8258017 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Gerrard; Wheelans
Journal of the Chemical Society, 1956 , p. 4296,4299 Full Text Show Details
T=87°C;
A
B
Synthesize Find similar
Synthesize Find similar
154
Synthesize Find similar Rx-ID: 8258018 Find similar reactions
Gerrard; Wheelans
Journal of the Chemical Society, 1956 , p. 4296,4299 Full Text Show Details
T=25°C;
A
B
Synthesize Find similar
Synthesize Find similar
155
Synthesize Find similar Rx-ID: 5687530 Find similar reactions
T=-15°C; unter Lichtausschluss;
Synthesize Find similar
Synthesize Find similar
Boehme; Schmitz
Chemische Berichte, 1955 , vol. 88, p. 357,361 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
156
Synthesize Find similar
Synthesize Find similar
Rx-ID: 5929159 Find similar reactions
Frazer; Gerrard
Journal of the Chemical Society, 1955 , p. 2959 Full Text Show Details
157
Synthesize Find similar
Rx-ID: 6218550 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Cade; Gerrard
Journal of the Chemical Society, 1954 , p. 2030,2033 Full Text Show Details
Mechanism;
A
B
Synthesize Find similar
Synthesize Find similar
158
Synthesize Find similar Rx-ID: 7061157 Find similar reactions
T=-60°C;
Synthesize Find similar
Synthesize Find similar
Douglass; Osborne
Journal of the American Chemical Society, 1953 , vol. 75, p. 4582 Full Text View citing articles Show Details
159
Synthesize Find similar
Synthesize Find similar
Rx-ID: 5929147 Find similar reactions
Wacker,A.
Patent: DE879554 , 1952 ;
T=800 - 900°C; beim Leiten durch ein Porzellanrohr;
Full Text Show Details
160
Synthesize Find similar
Rx-ID: 638790 Find similar reactions
Synthesize Find similar
Synthesize Find similar
With molybdenum oxide-tungsten oxide
T=200°C; unter Druck;
Du Pont de Nemours and Co.
Patent: US2700679 , 1951 ;
With copper oxide-tungsten oxide
T=200°C; unter Druck;
Du Pont de Nemours and Co.
Patent: US2700679 , 1951 ;
With nickel oxide; nickel oxide-molybdenum oxide
T=200°C; unter Druck;
Du Pont de Nemours and Co.
Patent: US2700679 , 1951 ;
Full Text Show Details
Full Text Show Details
Full Text Show Details
Hide Details
With aluminum oxide; silica gel
T=200°C; unter Druck;
Du Pont de Nemours and Co.
Patent: US2700679 , 1951 ; Full Text Show Details
A
B
161
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Rx-ID: 6683159 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Eastman Kodak Co.
Patent: US2475966 , 1945 ;
T=0°C; reagiert analog mit HBr und HI bei 10grad;
Full Text Show Details
Hagemeyer; Hull
Industrial and Engineering Chemistry, 1949 , vol. 41, p. 2921 Full Text Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
162
Synthesize Find similar
Synthesize Find similar
Rx-ID: 730094 Find similar reactions
Shepherd
Journal of Organic Chemistry, 1947 , vol. 12, p. 275,278, 280 Full Text View citing articles Show Details
T=230°C;
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
163
Synthesize Find similar Rx-ID: 730095 Find similar reactions
T=230°C;
Synthesize Find similar
Shepherd
Journal of Organic Chemistry, 1947 , vol. 12, p. 275,278, 280 Full Text View citing articles Show Details
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
164
Synthesize Find similar
Synthesize Find similar
Rx-ID: 7920616 Find similar reactions
Illari; Giuseppetti
Gazzetta Chimica Italiana, 1947 , vol. 77, p. 485,488, 489 Full Text Show Details
anschliessend Behandeln mit kaltem Wasser;
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
165
Synthesize Find similar
Synthesize Find similar
Rx-ID: 7920617 Find similar reactions
Illari; Giuseppetti
Gazzetta Chimica Italiana, 1947 , vol. 77, p. 485,488, 489 Full Text Show Details
anschliessend Behandeln mit kaltem Wasser;
A
B
Synthesize Find similar
Synthesize Find similar
166
Synthesize Find similar Rx-ID: 8265092 Find similar reactions
Synthesize Find similar
Bachman; Welton
Journal of Organic Chemistry, 1947 , vol. 12, p. 221,224 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
167
Synthesize Find similar
Synthesize Find similar
Rx-ID: 8265093 Find similar reactions
Bachman; Welton
Journal of Organic Chemistry, 1947 , vol. 12, p. 221,224 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
168
Synthesize Find similar Rx-ID: 26167835 Find similar reactions
169
Synthesize Find similar
in neat (no solvent) react. on mixing with acetic anhydride;;
Schmidt, H.; Blohm, C.; Jander, G.
Angewandte Chemie, 1947 , vol. 59, # A p. 233 - 237 Full Text Show Details
in neat (no solvent) react. on mixing with acetic anhydride;;
Ritter, H.
Liebigs Annalen der Chemie, 1855 , vol. 95, p. 208 - 211 Full Text Show Details
Gmelin Handbook: P: MVol.C, 196, page 449 - 451 Full Text Show Details
Synthesize Find similar
Synthesize Find similar
Rx-ID: 115867 Find similar reactions
With hydrogenchloride; diethyl ether
T=0°C;
Eastman Kodak Co.
Patent: US2475966 , 1945 ; Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
170
Synthesize Find similar Rx-ID: 26450009 Find similar reactions
With potassium chloride in liquid sulphur dioxide solvent: BF3 etherate;
Seel, F.
Z. Anorg. Chem., 1943 , vol. 250, p. 331 - 351 Full Text Show Details
With potassium chloride in further solvent(s) solvent: BF3 etherate;
Seel, F.
Z. Anorg. Chem., 1943 , vol. 250, p. 331 - 351 Full Text Show Details
With KCl in sulfur dioxide
solvent: BF3 etherate;
Gmelin Handbook: B: SVol.1, 4.4.5, page 187 - 196 Full Text Show Details
Hide Details
With KCl in further solvent(s) solvent: BF3 etherate;
Gmelin Handbook: B: SVol.1, 4.4.5, page 187 - 196 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
171
Synthesize Find similar Rx-ID: 5723388 Find similar reactions
T=10 - 15°C;
Synthesize Find similar
Synthesize Find similar
Weber; Hennion; Vogt
Journal of the American Chemical Society, 1939 , vol. 61, p. 1458 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
172
Synthesize Find similar
Synthesize Find similar
Rx-ID: 5929162 Find similar reactions
Wolnow
Zhurnal Obshchei Khimii, 1939 , vol. 9, p. 2269,2281 Chem. Zentralbl., 1940 , vol. 111, # I p. 2307 Full Text Show Details
T=110 - 120°C;
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
173
Synthesize Find similar
Synthesize Find similar
Rx-ID: 6219620 Find similar reactions
Wolnow
Zhurnal Obshchei Khimii, 1939 , vol. 9, p. 2269,2281 Chem. Zentralbl., 1940 , vol. 111, # I p. 2307 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
174
Synthesize Find similar Rx-ID: 7061155 Find similar reactions
Synthesize Find similar
Wolnow
Zhurnal Obshchei Khimii, 1939 , vol. 9, p. 2269,2281 Chem. Zentralbl., 1940 , vol. 111, # I p. 2307 Full Text Show Details
T=180 - 200°C;
A
B
Synthesize Find similar
Synthesize Find similar
175
Synthesize Find similar
Synthesize Find similar
Rx-ID: 7446030 Find similar reactions
Wolnow
Zhurnal Obshchei Khimii, 1939 , vol. 9, p. 2269,2281 Chem. Zentralbl., 1940 , vol. 111, # I p. 2307 Full Text Show Details
T=140°C;
A
B
Synthesize Find similar
Synthesize Find similar
176
Synthesize Find similar
Synthesize Find similar
Rx-ID: 7446031 Find similar reactions
Wolnow
Zhurnal Obshchei Khimii, 1939 , vol. 9, p. 2269,2281 Chem. Zentralbl., 1940 , vol. 111, # I p. 2307 Full Text Show Details
T=120°C;
A
B
Synthesize Find similar
Synthesize Find similar
177
Synthesize Find similar
Synthesize Find similar
Rx-ID: 26544609 Find similar reactions
Vol'nov, Yu. N.
Zhurnal obshchei Khim. (russ.), 1939 , vol. 9, p. 2269 - 2282 C. I, 1940 , p. 2307 Full Text Show Details
Gmelin Handbook: Si: MVol.C, 130, page 361 - 363 Full Text Show Details
distn.;;
178
Synthesize Find similar
Rx-ID: 615147 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Nessmejanow; Kahn
Chemische Berichte, 1934 , vol. 67, p. 370,372 Zhurnal Obshchei Khimii, 1934 , vol. 4, p. 1243,1245 Chem. Zentralbl., 1936 , vol. 107, # I p. 4287 Full Text Show Details
Brown
Journal of the American Chemical Society, 1938 , vol. 60, p. 1326 Full Text Show Details
179
Synthesize Find similar
Synthesize Find similar
Perrot
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1938 , vol. 206, p. 1576 Full Text Show Details
T=200°C;
A
180
Rx-ID: 5929151 Find similar reactions
B
Synthesize Find similar Rx-ID: 232560 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Kirrmann
Bulletin de la Societe Chimique de France, 1937 , vol. <5>4, p. 506 Bulletin de la Societe Chimique de France, 1938 , vol. <5>5, p. 258 Full Text Show Details
Erhitzen unter Athmosphaerendruck;
181
Synthesize Find similar
Synthesize Find similar
Rx-ID: 60183 Find similar reactions
With hydrogenchloride; carbon
Eschenbach
Patent: DE638441 , 1935 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 23, p. 74 Full Text Show Details
With hydrogenchloride
Chick; Wilsmore
Chem. Zentralbl., 1908 , vol. 79, # II p. 1018 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
182
Synthesize Find similar Rx-ID: 570480 Find similar reactions
Synthesize Find similar
Chem.Fabr.Weiler-ter Meer
Patent: DE350050 , 1920 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 14, p. 261 Full Text Show Details
Nessmejanow; Kahn
Chemische Berichte, 1934 , vol. 67, p. 370,372 Zhurnal Obshchei Khimii, 1934 , vol. 4, p. 1243,1245 Chem. Zentralbl., 1936 , vol. 107, # I p. 4287 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
183
Synthesize Find similar
Synthesize Find similar
Rx-ID: 642056 Find similar reactions
Nessmejanow; Kahn
Chemische Berichte, 1934 , vol. 67, p. 370,372 Zhurnal Obshchei Khimii, 1934 , vol. 4, p. 1243,1245 Chem. Zentralbl., 1936 , vol. 107, # I p. 4287 Full Text Show Details
T=100°C;
184
Synthesize Find similar
Rx-ID: 642057 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Nessmejanow; Kahn
Chemische Berichte, 1934 , vol. 67, p. 370,372 Zhurnal Obshchei Khimii, 1934 , vol. 4, p. 1243,1245 Chem. Zentralbl., 1936 , vol. 107, # I p. 4287 Full Text Show Details
T=100°C;
Nessmejanow; Kahn
Chemische Berichte, 1934 , vol. 67, p. 370,372 Zhurnal Obshchei Khimii, 1934 , vol. 4, p. 1243,1245 Chem. Zentralbl., 1936 , vol. 107, # I p. 4287 Full Text Show Details
With CoCl2
T=100°C;
Dow Chem.Co.
Patent: US1921767 , 1929 ; Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
185
Synthesize Find similar
Synthesize Find similar
Rx-ID: 642058 Find similar reactions
Nessmejanow; Kahn
Chemische Berichte, 1934 , vol. 67, p. 370,372 Zhurnal Obshchei Khimii, 1934 , vol. 4, p. 1243,1245 Chem. Zentralbl., 1936 , vol. 107, # I p. 4287 Full Text Show Details
T=100°C;
186
Synthesize Find similar
Rx-ID: 555227 Find similar reactions
Synthesize Find similar
Synthesize Find similar
With zinc(II) chloride
Monsanto Chem.Co.
Patent: US2051096 , 1933 ;
Full Text Show Details
187
Synthesize Find similar
Rx-ID: 638797 Find similar reactions
T=250°C; Leiten ueber Phosphortorfkohle;
Synthesize Find similar
Synthesize Find similar
I.G. Farbenind.
Patent: DE638306 , 1932 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 21, p. 161 Full Text Show Details
With kieselguhr; magnesium chloride
T=160 - 170°C;
I.G.Farbenind.
Patent: DE655683 , 1933 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 23, p. 72 Full Text Show Details
I.G.Farbenind.
Patent: US2013988 , 1933 ; Full Text Show Details
I.G.Farbenind.
Patent: FR754986 , 1933 ; Full Text Show Details
Hide Details
With magnesium oxide
T=80 - 110°C;
I.G.Farbenind.
Patent: US2013988 , 1933 ; Full Text Show Details
I.G.Farbenind.
Patent: FR754986 , 1933 ; Full Text Show Details
With kieselguhr; CaO
T=160 - 170°C;
I.G.Farbenind.
Patent: DE655683 , 1933 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 23, p. 72 Full Text Show Details
With phosphorus peat-coal
T=250°C;
I.G.Farbenind.
Patent: DE638306 , 1932 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 21, p. 161 Full Text Show Details
I.G.Farbenind.
Patent: US2013989 , 1933 ; Full Text Show Details
T=110 - 120°C;
Kempf
Journal fuer Praktische Chemie (Leipzig), 1870 , vol. <2> 1, p. 412 Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften, 1870 , p. 396 Full Text Show Details
With lithium chloride
T=140°C;
I.G.Farbenind.
Patent: DE655683 , 1933 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 23, p. 72 Full Text Show Details
With Magnesium acetate
T=80 - 110°C;
I.G.Farbenind.
Patent: US2013988 , 1933 ; Full Text Show Details
I.G.Farbenind.
Patent: FR754986 , 1933 ; Full Text Show Details
T=110 - 120°C;
Kempf
Journal fuer Praktische Chemie (Leipzig), 1870 , vol. <2> 1, p. 412 Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften, 1870 , p. 396 Full Text Show Details
188
Synthesize Find similar
Synthesize Find similar
Rx-ID: 646911 Find similar reactions
With nickel dichloride
T=110°C; beim Chlorieren;
Akashi
Bl.Inst.phys.chem.Res.Abstr.Tokyo, 1933 , vol. 6, p. 22 Chem. Zentralbl., 1933 , vol. 104, # I p. 3066 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
189
Synthesize Find similar Rx-ID: 6208896 Find similar reactions
Akashi
Bl. Inst. phys. chem. Res. Abstr. Tokyo, vol. 6, p. 22 Chem. Zentralbl., 1933 , vol. 104, # I p. 3066 Full Text Show Details
T=110°C; Chlorieren in der Dampfphase;
A
B
Synthesize Find similar
Synthesize Find similar
190
Synthesize Find similar Rx-ID: 7918944 Find similar reactions
Synthesize Find similar
Hurd; Thomas
Journal of the American Chemical Society, 1933 , vol. 55, p. 275,281 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
191
Synthesize Find similar
Synthesize Find similar
Rx-ID: 26148960 Find similar reactions
dropping of BCl3 to acetic acid anhydride in cooling;
Meerwein, H.; Maier-Hueser, H.
Journal fuer Praktische Chemie (Leipzig), 1932 , vol. 134, p. 51 - 81 Full Text Show Details
dropping of BCl3 to acetic acid anhydride in cooling;
Gmelin Handbook: B: SVol.1, 4.5, page 196 - 204 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
192
Synthesize Find similar Rx-ID: 238434 Find similar reactions
Gibson
Chemistry and Industry (London, United Kingdom), 1931 , p. 949,970 Chem. Zentralbl., 1932 , vol. 103, # I p. 2009 Full Text Show Details
beim Stehenlassen;
193
Synthesize Find similar
Synthesize Find similar
T=860°C; durch ein mit Kupfer ausgekleidetes Stahlrohr (Kontaktzeit:0.29 sec);
Rx-ID: 5929150 Find similar reactions
Standard Oil Devel.Co.
Patent: US2062344 , 1931 ;
Full Text Show Details
Standard Oil Devel.Co.
Patent: US2062344 , 1931 ;
T=500°C; P=88260.9 Torr; durch ein mit Kupfer ausgekleidetes Stahlrohr;
Full Text Show Details
With NaPO3
T=700 - 800°C; zweckmaessig unter Druck;
I.G.Farbenind.
Patent: DE561399 , 1928 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 18, p. 231 Full Text Show Details
Hide Details
With anhydrous sodium borate
T=700 - 800°C; zweckmaessig unter Druck;
I.G.Farbenind.
Patent: DE561399 , 1928 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 18, p. 231 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
194
Synthesize Find similar Rx-ID: 227331 Find similar reactions
Soc. Usines Chim. Rhone-Poulenc
Patent: DE527874 , 1929 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 18, p. 232,796 Full Text Show Details
Soc. Usines Chim. Rhone-Poulenc
Patent: DE531156 , 1930 ;
T=380 - 400°C;
Full Text Show Details
Soc. Usines Chim. Rhone-Poulenc
Patent: DE527874 , 1929 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 18, p. 232,796 Full Text Show Details
Soc. Usines Chim. Rhone-Poulenc
Patent: DE531156 , 1930 ;
T=250 - 300°C; beim Ueberleiten ueber Bimsstein;
Full Text Show Details
A
195
B
Synthesize Find similar
Synthesize Find similar
Rx-ID: 6682572 Find similar reactions
With pumice stone
T=250°C;
Soc.Usines Chim.Rhone-Poulene
Patent: DE527874 , 1929 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 18, p. 232,796 Full Text Show Details
Soc.Usines Chim.Rhone-Poulene
Patent: DE531156 , 1930 ; Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
196
Synthesize Find similar Rx-ID: 6682573 Find similar reactions
Soc. Usines Chim. Rhone-Poulenc
Patent: DE527874 , 1929 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 18, p. 232,796 Full Text Show Details
Soc. Usines Chim. Rhone-Poulenc
Patent: DE531156 , 1930 ;
T=250°C;
Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
197
Synthesize Find similar Rx-ID: 7065198 Find similar reactions
Soc. Usines Chim. Rhone-Poulenc
Patent: DE527874 , 1929 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 18, p. 232,796 Full Text Show Details
Soc. Usines Chim. Rhone-Poulenc
Patent: DE531156 , 1930 ;
T=80 - 130°C;
Full Text Show Details
198
Synthesize Find similar
Rx-ID: 571075 Find similar reactions
T=80°C;
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Rabcewicz-Zubkowski
Roczniki Chemii, vol. 9, p. 529 Chem. Zentralbl., 1929 , vol. 100, # II p. 2767 Full Text Show Details