1.4 Piperidine

Page 1

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PubChem

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Reactions (526)

Yield

Substances (1)

Citations (573)

Conditions

References

298

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Rx-ID: 1642133 Find similar reactions

Nichols, Peter J.; Grant, Michael W.

Australian Journal of Chemistry, 1982 , vol. 35, # 12 p. 2455 - 2463 Title/Abstract Full Text Show Details

With strong acid; sodium perchlorate in water

T=25°C; Rate constant;

A

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Rx-ID: 1783872 Find similar reactions

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Bamkole, Titus O.; Hirst, Jack; Onyido, Ikenna

Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1982 , p. 889 - 894 Title/Abstract Full Text Show Details

in benzene

other solvent; Equilibrium constant;

A

B

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300

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Alberola, A.; Gonzalez, A. M.; Guerra, D.; Pulido, F. J.

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 1073 - 1076 Title/Abstract Full Text Show Details

Heatingdecomposition in the mass spectrophotometer; Product distribution;

A

B

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301

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Alberola, A.; Gonzalez, A. M.; Guerra, D.; Pulido, F. J.

Journal of Heterocyclic Chemistry, 1982 , vol. 19, p. 1073 - 1076 Title/Abstract Full Text Show Details

Heatingdecomposition in the mass spectrophotometer; Product distribution;

A

302

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With water in dimethyl sulfoxide

Equilibrium constant;

Rossi, Rita H. de; Nunez, Alberto

Journal of Organic Chemistry, 1982 , vol. 47, # 2 p. 319 - 325 Title/Abstract Full Text View citing articles Show Details

A

B

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303

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With water in propan-1-ol

T=25°C; Rate constant;

Novikov, V. N.; Borodaev, S. V.; Babeshkina, L. D.

Chemistry of Heterocyclic Compounds (New York, NY, United States), 1982 , p. 448 - 454 Khimiya Geterotsiklicheskikh Soedinenii, 1982 , vol. 18, # 5 p. 601 - 609 Title/Abstract Full Text View citing articles Show Details

A

B

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304

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With tetrahydropyridine hydrochloride in dimethyl sulfoxide

T=25°C; Equilibrium constant;

Brooke, David N.; Crampton, Michael R.

Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1982 , p. 231 - 238 Title/Abstract Full Text Show Details

A

305

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With tetrahydropyridine hydrochloride in dimethyl sulfoxide

T=25°C; Equilibrium constant;

Brooke, David N.; Crampton, Michael R.

Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1982 , p. 231 - 238 Title/Abstract Full Text Show Details

A

B

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306

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Muralikrishna, U; Krishnamurthy, Mannam

Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 11 p. 1018 - 1020 Title/Abstract Full Text Show Details

in chloroform

Equilibrium constant;

A

B

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307

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in chloroform

Equilibrium constant;

Muralikrishna, U; Krishnamurthy, Mannam

Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 11 p. 1018 - 1020 Title/Abstract Full Text Show Details


A

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308

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Muralikrishna, U; Krishnamurthy, Mannam

Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1982 , vol. 21, # 11 p. 1018 - 1020 Title/Abstract Full Text Show Details

in chloroform

Equilibrium constant;

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B

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309

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Rx-ID: 1783870 Find similar reactions

Ellenberger, Mark R.; Dixon, David A.; Farneth, William E.

Journal of the American Chemical Society, 1981 , vol. 103, # 18 p. 5377 - 5382 Title/Abstract Full Text View citing articles Show Details

ICR double resonance, proton affinity;

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310

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ICR double resonance, proton affinity;

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Ellenberger, Mark R.; Dixon, David A.; Farneth, William E.

Journal of the American Chemical Society, 1981 , vol. 103, # 18 p. 5377 - 5382 Title/Abstract Full Text View citing articles Show Details


A

B

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311

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With water

Eicher, Thoephil; Franke, Guenter

Liebigs Annalen der Chemie, 1981 , # 8 p. 1337 - 1353 Title/Abstract Full Text Show Details

A

B

C

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312

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With sulfuric acid; chloramine-T in water; acetic acid

0.25 h; Ambient temperaturequantitative determination of the title compound; Product distribution;

Yusuff, K. K. M.; Gopalan, M.

Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical, 1981 , vol. 20, # 8 p. 859 Title/Abstract Full Text Show Details

A

B

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313

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in dimethyl sulfoxide

T=25°C; kinetic of reactions of cyclic secondary amines (pyrrolidine, piperidine) with 2,4-dinitro-1-naphthyl ethyl ether in DMSO; stage I kinetics and equilibrium (with piperidine); Rate constantEquilibrium constantMechanism;

Bunnett, Joseph F.; Sekiguchi, Shizen; Smith, Lewis A.

Journal of the American Chemical Society, 1981 , vol. 103, # 16 p. 4865 - 4871 Title/Abstract Full Text View citing articles Show Details


A

B

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314

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With tetrahydropyridine hydrochloride in dimethyl sulfoxide

T=25°C; reversible reactions of amines with the corresponding N-(2,4-dinitro-1-naphthylamines); difference between pyrrolidine and piperidine systems; Equilibrium constantMechanism;

Sekiguchi, Shizen; Bunnett, J. F.

Journal of the American Chemical Society, 1981 , vol. 103, # 16 p. 4871 - 4874 Title/Abstract Full Text View citing articles Show Details

315

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Rx-ID: 20625318 Find similar reactions

Multi-step reaction with 3 steps 1: 69 percent / toluene 2: 81 percent / H2O of air / 2160 h 3: H2O View Scheme

Eicher, Thoephil; Franke, Guenter

Liebigs Annalen der Chemie, 1981 , # 8 p. 1337 - 1353 Title/Abstract Full Text Show Details

316

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Multi-step reaction with 2 steps 1: 81 percent / H2O of air / 2160 h 2: H2O View Scheme

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Rx-ID: 20636184 Find similar reactions

Eicher, Thoephil; Franke, Guenter

Liebigs Annalen der Chemie, 1981 , # 8 p. 1337 - 1353 Title/Abstract Full Text Show Details


A

B

C

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317

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Rx-ID: 1500319 Find similar reactions

A: 20% B: 15% C: 50%

With Ps(acac)2; triethylaluminum; triphenylphosphine in toluene

6 h; Heating;

Dzhemilev, U. M.; Selimov, F. A.; Tolstikov, G. A.

Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1980 , vol. 29, # 2 p. 263 - 266 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1980 , # 2 p. 348 - 352 Title/Abstract Full Text View citing articles Show Details

A

B

C

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318

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A: 50% B: 20%

With bis(acetylacetonato) palladium; triethylaluminum; triphenylphosphine in toluene

T=100°C; 4 h;

Dzhemilev, U. M.; Selimov, F. A.; Tolstikov, G. A.

Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation), 1980 , vol. 29, # 2 p. 263 - 266 Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1980 , # 2 p. 348 - 352 Title/Abstract Full Text View citing articles Show Details

A

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D

E

F

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319

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With hydrogen; sulphidized CoO-MoO3

T=300°C; P=37503 Torr; 1 h; prolonged (9 h) heating affords additional N-(1-butyl)piperidine, N-(1-ethyl)piperidine, and decane; MechanismProduct distribution;

Cerny, Mirko

Collection of Czechoslovak Chemical Communications, 1980 , vol. 45, # 8 p. 2215 - 2218 Title/Abstract Full Text Show Details


A

B

C

D

E

F

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320

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A: 5.4% B: 5.8% C: 0.8% D: 3%

With hydrogen; sulphidized CoO-MoO3

T=300°C; P=45003.6 - 90757.2 Torr; 8 h; MechanismProduct distribution;

Cerny, Mirko

Collection of Czechoslovak Chemical Communications, 1980 , vol. 45, # 8 p. 2215 - 2218 Title/Abstract Full Text Show Details

A

B

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321

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With formic acid in various solvent(s) T=0°C; var. solvents; Rate constant;

Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru

Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details

A

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322

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With formic acid in various solvent(s)

Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru


T=0°C; var. solvents; Rate constant;

Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details

A

B

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323

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With formic acid in various solvent(s) T=0°C; var. solvents; Rate constant;

Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru

Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details

A

B

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324

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With formic acid in various solvent(s) T=0°C; var. solvents; Rate constant;

Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru

Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details

A

B

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325

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With formic acid in various solvent(s) T=0°C; var. solvents; Rate constant;

Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru

Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details

A

B

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326

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With formic acid in toluene

T=0°C; var. solvents and reagent ratio,; Rate constantMechanism;

Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru

Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details

A

B

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327

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With formic acid in various solvent(s) T=0°C; var. solvents; Rate constant;

Fukawa, Hidemichi; Suzuki, Kunio; Sekiya, Minoru

Chemical & Pharmaceutical Bulletin, 1980 , vol. 28, # 10 p. 2868 - 2873 Title/Abstract Full Text Show Details

A

B

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328

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Falk, Heinz; Mueller, Norbert; Schlederer, Thomas

Monatshefte fuer Chemie, 1980 , vol. 111, p. 159 - 176 Title/Abstract Full Text View citing articles Show Details

in dimethyl sulfoxide

T=22°C; temperature-dependence and solvent-dependence of the equilibrium; Equilibrium constant;

A

B

C

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329

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With water

T=37°C; Rate constant;

Bundgaard; Johansen

Journal of Pharmaceutical Sciences, 1980 , vol. 69, # 1 p. 44 - 46 Title/Abstract Full Text View citing articles Show Details

A

B

C

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330

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With water

T=37°C; Rate constant;

Bundgaard; Johansen

Journal of Pharmaceutical Sciences, 1980 , vol. 69, # 1 p. 44 - 46 Title/Abstract Full Text View citing articles Show Details

A

B

C

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331

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With water

T=37°C; Rate constant;

Bundgaard; Johansen

Journal of Pharmaceutical Sciences, 1980 , vol. 69, # 1 p. 44 - 46 Title/Abstract Full Text View citing articles Show Details

A

B

C

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332

Synthesize Find similar Rx-ID: 4019439 Find similar reactions

With water

T=37°C; Rate constant;

Bundgaard; Johansen

Journal of Pharmaceutical Sciences, 1980 , vol. 69, # 1 p. 44 - 46 Title/Abstract Full Text View citing articles Show Details

A

B

C

D

E

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333

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With Fe2(CO)9 in benzene

T=45°C; 2 h; var. reaction partners and times; other N-alkyloxyamines; Product distributionMechanism;

A

B

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334

Rx-ID: 25355180 Find similar reactions

Blum, Y.; Becker, Y.; Shvo, Y.

Journal of Organometallic Chemistry, 1980 , vol. 202, # 1 p. 65 - 76 Title/Abstract Full Text View citing articles Show Details


E. I. Du Pont de Nemours and Company

Patent: US4220608 A1, 1980 ;

Hide Experimental Procedure

Title/Abstract Full Text Show Details

9:HF and Piperidine

HF and Piperidine The procedure of Example 4 was repeated, using 12.8 g (0.15 mole) of piperidine in place of quinoline, and gave 1.5 g of 3,3,3-trifluoropropene-1. A

B

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335

Rx-ID: 25283140 Find similar reactions

Gruppo Lepetit S.p.A.

Patent: US4129562 A1, 1978 ;

Hide Experimental Procedure

Title/Abstract Full Text Show Details

5:4-desoxy-2'-(piperidino)carbonyl-thiazolo[5,4-c]rifamycin SV

EXAMPLE 5 4-desoxy-2'-(piperidino)carbonyl-thiazolo[5,4-c]rifamycin SV The compound of the title was prepared according to the procedure of Example 3 from the compound of Example 1 and piperidine (M.p. 175°-178° C. with decomposition). A

B

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336

A: 65%

Rx-ID: 25209957 Find similar reactions

Societa' Farmaceutici Italia S.p.A.

Patent: US4024224 A1, 1977 ;

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Title/Abstract Full Text Show Details

3:14-(N-piperidino)-daunomycin

EXAMPLE 3 14-(N-piperidino)-daunomycin By following the procedures described in Example 1, but using an equivalent amount of piperidine instead of morpholine, 14-(N-piperidino)-daunomycin monohydrochloride was obtained; E1.2 = 1.7; E1 cm.1percent = 192 at 495 nm. (yield = 65percent). A

B


337

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Rx-ID: 25209958 Find similar reactions

Boehringer Ingelheim GmbH

Patent: US4021551 A1, 1977 ;

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Title/Abstract Full Text Show Details

24:EXAMPLE 24

EXAMPLE 24 Using a procedure analogous to that described in Example 23, 78percent of theory of 3,6-bis-[(α-piperidino-butyryl)-amino]-acridine hemihydrate, m.p. 103°-106° C. (recrystallized from ethanol/water), was obtained from 3,6-bis-(α-chlorobutyryl-amino)-acridine and piperidine. A

B

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338

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Boehringer Ingelheim GmbH

Patent: US4021551 A1, 1977 ;

Hide Experimental Procedure

Title/Abstract Full Text Show Details

19:EXAMPLE 19

EXAMPLE 19 Using a procedure analogous to that described in Example 18, 68percent of theory of 3,6-bis-[α-(piperidino)-propionyl-amino]-acridine hydrate, m.p. 197°-201° C. (recrystallized from ethanol), was obtained from 3,6-bis-(α-chloropropionyl-amino)-acridine and piperidine. A

B

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339

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Rx-ID: 25282736 Find similar reactions

Boehringer Ingelheim GmbH

Patent: US4021551 A1, 1977 ;

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Title/Abstract Full Text Show Details

31:EXAMPLE 31

EXAMPLE 31 Using a procedure analogous to that described in Example 30, 70.9percent of theory of 3,6-bis-[(α-piperidino-isobutyryl)-amino]-acridine trihydrate, m.p. 131°-137° C. (recrystallized from ethanol), was obtained from 3,6-bis-(α-chloroisobutyryl-amino)-acridine and piperidine. A

B

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340

Rx-ID: 25209956 Find similar reactions

Richardson-Merrell Inc.

Patent: US3946021 A1, 1976 ;

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Title/Abstract Full Text Show Details

16:EXAMPLE 16

EXAMPLE 16 Following the procedure of Example 15, only substituting for dimethylaminie an excess amount of diethylamine and piperidine, the following compounds are prepared.

341

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Rx-ID: 25258804 Find similar reactions

With triethylamine

Mitsui Toatsu Chemicals, Incorporated

Patent: US3994932 A1, 1976 ;

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Title/Abstract Full Text Show Details

17:EXAMPLE 17

When the process was repeated using 60 grams of triethylamine or 52 grams of morpholine instead of the piperidine, similar results were obtained. A

B


342

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Rx-ID: 26730925 Find similar reactions

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Stynes; James

Journal of the American Chemical Society, 1974 , vol. 96, # 9 p. 2733 - 2738 Title/Abstract Full Text View citing articles Show Details

in toluene

Kinetics; 23°C;

Gmelin Handbook: Fe: Org.Verb.B1, 1.1.4.1.6.4.2.2, page 77 - 79 Full Text Show Details

A

B

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343

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Rx-ID: 90979 Find similar reactions

Zehrung; Woodburn

Journal of Organic Chemistry, 1959 , vol. 24, p. 1333 Full Text View citing articles Show Details

A

B

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344

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Zehrung; Woodburn


Journal of Organic Chemistry, 1959 , vol. 24, p. 1333 Full Text View citing articles Show Details

A

B

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345

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Rx-ID: 5404829 Find similar reactions

Ferles

Collection of Czechoslovak Chemical Communications, 1959 , vol. 24, p. 1029,1031, 1033 Full Text Show Details

bei der elektrochemischen Reduktion;

A

B

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346

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Rx-ID: 5411992 Find similar reactions

Zahradnik; Zuman

Collection of Czechoslovak Chemical Communications, 1959 , vol. 24, p. 1132,1136 Full Text Show Details

T=20 - 36°C; Zersetzung in gepufferten wss. Loesungen vom pH 4,1-5,8; Rate constant;

347

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Rx-ID: 8427187 Find similar reactions

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Zehrung; Woodburn


Journal of Organic Chemistry, 1959 , vol. 24, p. 1333 Full Text View citing articles Show Details

348

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Rx-ID: 5403481 Find similar reactions

Hales; Herington

Transactions of the Faraday Society, 1957 , vol. 53, p. 616,621 Full Text Show Details

T=140 - 260°C; Equilibrium constant;

349

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Rx-ID: 5742329 Find similar reactions

Schuikin; Tulupow

Vestnik Moskovskogo Universiteta, 1956 , vol. 11, # 3 p. 73,74 Chem.Abstr., 1956 , p. 12446 Full Text Show Details

T=150°C; Hydrogenation;

350

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Rx-ID: 222258 Find similar reactions

With kieselguhr; ammonia; cobalt

T=170°C; P=191232 Torr; Hydrogenation;

ICI

Patent: US2790804 , 1955 ;

With ammonia; nickel

ICI

Full Text Show Details


Patent: US2790804 , 1955 ;

T=170°C; P=147102 Torr; Hydrogenation;

Full Text Show Details

351

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Rx-ID: 5403465 Find similar reactions

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Reppe et al.

Justus Liebigs Annalen der Chemie, 1955 , vol. 596, p. 65 Full Text Show Details

T=310°C;

A

B

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352

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I.G. Farbenind.

Patent: DE765203 , 1939 ; DRP/DRBP Org.Chem. Full Text Show Details

Reppe et al.

Justus Liebigs Annalen der Chemie, 1955 , vol. 596, p. 162,182 Full Text Show Details

T=250°C;

A

B

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353

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Rx-ID: 824655 Find similar reactions

With sodium

T=165°C;

Terent'ew; Jaschunskii

Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 291,296; engl. Ausg. S. 295, 298 Full Text Show Details

A

B

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354

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Kroehnke; Vogt

Justus Liebigs Annalen der Chemie, 1954 , vol. 589, p. 52 Full Text Show Details

A

B

C

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355

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Rx-ID: 7053304 Find similar reactions

Terent'ew; Jaschunskii

Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 291,296; engl. Ausg. S. 295, 298 Full Text Show Details

A

B

C

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356

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Rx-ID: 7053305 Find similar reactions

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Terent'ew; Jaschunskii

Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 291,296; engl. Ausg. S. 295, 298 Full Text Show Details

A

B

C

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357

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Rx-ID: 7053306 Find similar reactions

Terent'ew; Jaschunskii

Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 291,296; engl. Ausg. S. 295, 298 Full Text Show Details

A

B

C

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358

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Rx-ID: 7053307 Find similar reactions

Terent'ew; Jaschunskii

Zhurnal Obshchei Khimii, 1954 , vol. 24, p. 291,296; engl. Ausg. S. 295, 298 Full Text Show Details

A

359

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B


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Rx-ID: 5673491 Find similar reactions

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Micovic; Mihailovic

Journal of Organic Chemistry, 1953 , vol. 18, p. 1190,1196 Full Text Show Details

Mousseron et al.

Bulletin de la Societe Chimique de France, 1952 , p. 1042,1052 Bulletin de la Societe Chimique de France, 1954 , p. 1246,1251 Full Text Show Details

T=-15°C; weniger als 1 Mol LiAlH4;

360

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Rx-ID: 166100 Find similar reactions

With sodium hydroxide; water

Bourns; Tudge

Canadian Journal of Chemistry, 1952 , vol. 30, p. 7371 Full Text Show Details

A

B

C

D

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361

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T=400°C;

Malinowskii; Morgun

Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1952 , vol. 25, p. 333;engl.Ausg.S.367 Full Text View citing articles Show Details

T=450°C;

Malinowskii; Morgun

Zhurnal Prikladnoi Khimii (Sankt-Peterburg, Russian Federation), 1952 , vol. 25, p. 333;engl.Ausg.S.367 Full Text View citing articles Show Details

A

B


362

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Rx-ID: 5469317 Find similar reactions

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Mousseron et al.

Bulletin de la Societe Chimique de France, 1952 , p. 1042,1052 Bulletin de la Societe Chimique de France, 1954 , p. 1246,1251 Full Text Show Details

T=-15°C; weniger als 1 Mol LiAlH4;

A

B

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Synthesize Find similar

363

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5711573 Find similar reactions

Mousseron et al.

Bulletin de la Societe Chimique de France, 1952 , p. 1042,1052 Bulletin de la Societe Chimique de France, 1954 , p. 1246,1251 Full Text Show Details

T=-15°C; weniger als 1 Mol LiAlH4;

A

B

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Synthesize Find similar

364

Synthesize Find similar Rx-ID: 5746102 Find similar reactions

Synthesize Find similar

Kloosterziel et al.

Recueil des Travaux Chimiques des Pays-Bas, 1952 , vol. 71, p. 1231,1233 Full Text View citing articles Show Details


A

B

Synthesize Find similar

Synthesize Find similar

365

Synthesize Find similar Rx-ID: 5408375 Find similar reactions

Sumitomo; Hachihama

Kogyo Kagaku Zasshi, 1951 , vol. 54, p. 199 Chem.Abstr., 1953 , p. 8060 Full Text Show Details

T=300 - 350°C; Hydrogenation;

A

B

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Synthesize Find similar

366

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5474881 Find similar reactions

Protiva; Jilek

Collection of Czechoslovak Chemical Communications, 1951 , vol. 16/17, p. 151 Full Text Show Details

A

B

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Synthesize Find similar

367

Synthesize Find similar Rx-ID: 5474882 Find similar reactions

T=130°C;

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Protiva; Jilek


Collection of Czechoslovak Chemical Communications, 1951 , vol. 16/17, p. 151 Full Text Show Details

368

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Rx-ID: 5685330 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Galinovsky et al.

Monatshefte fuer Chemie, 1951 , vol. 82, p. 551,557 Full Text Show Details

369

Synthesize Find similar

Rx-ID: 5403478 Find similar reactions

Synthesize Find similar

Synthesize Find similar

De Mayo; Rigby

Nature (London, United Kingdom), 1950 , vol. 166, p. 1075 Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

370

Synthesize Find similar Rx-ID: 222259 Find similar reactions

With ethanol; ammonia; nickel

T=110 - 150°C; P=58840.6 Torr; Hydrogenation;

Crum; Robinson

Journal of the Chemical Society, 1943 , p. 561,562


Full Text Show Details

With ammonia; cobalt

T=80 - 100°C; Hydrogenation;

I.G. Farbenind.

BIOS Final Rep. Nr. 350 <1946> Full Text Show Details

Reppe,W.

Acetylene Chemistry <New York 1949> S. 123 Full Text Show Details

Reppe

Experientia, 1949 , vol. 5, p. 93,108 Justus Liebigs Annalen der Chemie, 1953 , vol. 582, p. 1,16, 35 Full Text Show Details

371

Synthesize Find similar

Rx-ID: 5403467 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Szmaragd; Briner

Helvetica Chimica Acta, 1949 , vol. 32, p. 553,560 Full Text Show Details

bei der elektrochemischen Reduktion;

372

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Rx-ID: 5403476 Find similar reactions

373

bei der elektrochemischen Reduktion;

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Szmaragd; Briner

Helvetica Chimica Acta, 1949 , vol. 32, p. 553,560 Full Text Show Details


Synthesize Find similar

Rx-ID: 6798919 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Reppe,W.

Acetylene Chemistry <New York 1949> S. 98, 123 Full Text Show Details

Adkins; Cramer

Journal of the American Chemical Society, 1930 , vol. 52, p. 4349,4354 Full Text Show Details

Reppe

Experientia, 1949 , vol. 5, p. 93,108 Justus Liebigs Annalen der Chemie, 1953 , vol. 582, p. 1,16, 35 Full Text Show Details

T=110 - 150°C; P=58840.6 - 73550.8 Torr; Hydrogenation;

A

B

C

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

374

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5704179 Find similar reactions

Schoepf et al.

Justus Liebigs Annalen der Chemie, 1948 , vol. 559, p. 1,22, 23 Chemische Berichte, 1951 , vol. 84, p. 690,698 Full Text Show Details

Hydrogenation;

375

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T=300°C;

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Rx-ID: 6798916 Find similar reactions

Scriabine


Bulletin de la Societe Chimique de France, 1947 , p. 454 Full Text Show Details

376

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Rx-ID: 5403464 Find similar reactions

With water; hydrogen bromide

Woods; Sanders

Journal of the American Chemical Society, 1946 , vol. 68, p. 2111 Full Text View citing articles Show Details

377

Synthesize Find similar

Rx-ID: 6798914 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Woods; Sanders

Journal of the American Chemical Society, 1946 , vol. 68, p. 2111 Full Text View citing articles Show Details

A

B

Synthesize Find similar

Synthesize Find similar

378

Synthesize Find similar Rx-ID: 5408376 Find similar reactions

T=140 - 215°C; P=102971 Torr; Hydrogenation;

Wilson

Journal of the American Chemical Society, 1945 , vol. 67, p. 693 Full Text View citing articles Show Details


379

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Rx-ID: 5403466 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Kline; Turkevich

Journal of the American Chemical Society, 1944 , vol. 66, p. 1710,1714 Full Text View citing articles Show Details

Jur'ew et al.

Zhurnal Obshchei Khimii, 1939 , vol. 9, p. 590,593 Chem. Zentralbl., 1940 , vol. 111, # II p. 902 Full Text Show Details

T=400 - 430°C;

A

B

C

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Synthesize Find similar

Synthesize Find similar

380

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5404665 Find similar reactions

Kline; Turkevich

Journal of the American Chemical Society, 1944 , vol. 66, p. 1710,1714 Full Text View citing articles Show Details

T=400°C;

A

B

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Synthesize Find similar

381

Synthesize Find similar Rx-ID: 19543 Find similar reactions

With kieselguhr; nickel

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Sawa et al.


T=200°C; P=55163.1 Torr; Hydrogenation;

Yakugaku Zasshi, 1943 , vol. 63, p. 319,324 Chem.Abstr., 1951 , p. 2940 Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

382

Synthesize Find similar

Synthesize Find similar

Rx-ID: 22209 Find similar reactions

With kieselguhr; nickel

T=220°C; P=64724.7 Torr; Hydrogenation;

Sawa et al.

Yakugaku Zasshi, 1943 , vol. 63, p. 319,324 Chem.Abstr., 1951 , p. 2940 Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

383

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Rx-ID: 288800 Find similar reactions

Dupont

Bulletin des Societes Chimiques Belges, 1942 , vol. 51, p. 209,220 Full Text Show Details

With piperidine; diethyl ether; xylene

anschliessend Behandeln mit HClO4;

384

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T=130 - 250°C; P=51485.6 - 102971 Torr; Hydrogenation;

Synthesize Find similar

Rx-ID: 5403468 Find similar reactions

Bergstrom; Carson


Journal of the American Chemical Society, 1941 , vol. 63, p. 2934 Full Text View citing articles Show Details

385

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Synthesize Find similar

Rx-ID: 5403479 Find similar reactions

Bergstrom; Carson

Journal of the American Chemical Society, 1941 , vol. 63, p. 2934 Full Text View citing articles Show Details

T=130 - 250°C; P=51485.6 - 102971 Torr; Hydrogenation;

386

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5403487 Find similar reactions

Bergstrom; Carson

Journal of the American Chemical Society, 1941 , vol. 63, p. 2934 Full Text View citing articles Show Details

T=130 - 250°C; P=51485.6 - 102971 Torr; Hydrogenation;

387

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5403488 Find similar reactions

Bergstrom; Carson

Journal of the American Chemical Society, 1941 , vol. 63, p. 2934 Full Text View citing articles Show Details

T=130 - 250°C; P=51485.6 - 102971 Torr; Hydrogenation;

A

B

C


388

Synthesize Find similar

Synthesize Find similar

Rx-ID: 5462953 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Mannich; Kniss

Chemische Berichte, 1941 , vol. 74, p. 1641 Full Text View citing articles Show Details

Anschliessend weitere Hydrierung an Palladium/Kohle in Aethanol..Hydrogenation;

389

Synthesize Find similar

Synthesize Find similar

Rx-ID: 8274861 Find similar reactions

Mannich; Hoenig

Archiv der Pharmazie (Weinheim, Germany), 1927 , p. 601 Full Text Show Details

Dimroth; Resin; Zetzsch

Chemische Berichte, 1940 , vol. 73, p. 1399,1404 Full Text Show Details

T=170°C;

A

B

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Synthesize Find similar

390

Synthesize Find similar Rx-ID: 17377 Find similar reactions

With ammonia; hydrogen; nickel

T=450°C; P=22065.2 Torr;

Gen. Aniline and Film Corp.

Patent: US2265201 , 1939 ; Full Text Show Details


391

Synthesize Find similar

Rx-ID: 30376 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Gen. Aniline and Film Corp.

Patent: US2265201 , 1939 ;

With ammonia

T=150 - 250°C; P=147102 Torr; Hydrogenation.an einem Kobalt-Katalysator;

Full Text Show Details

I.G. Farbenind.

Patent: DE695472 , 1938 ; DRP/DRBP Org.Chem. Full Text Show Details

A

B

Synthesize Find similar

Synthesize Find similar

392

Synthesize Find similar Rx-ID: 106801 Find similar reactions

With 1,4-dioxane; nickel

T=225°C; Hydrogenation;

D'Ianni; Adkins

Journal of the American Chemical Society, 1939 , vol. 61, p. 1675,1676 Full Text Show Details

393

Synthesize Find similar

Synthesize Find similar

With ammonia

T=250°C; P=147102 Torr; Hydrogenation.an einen Kobalt-Katalysator;

Rx-ID: 161189 Find similar reactions

Gen. Aniline and Film Corp.

Patent: US2265201 , 1939 ;


Full Text Show Details

I.G. Farbenind.

Patent: DE695472 , 1938 ; DRP/DRBP Org.Chem. Full Text Show Details

Gen. Aniline and Film Corp.

Patent: US2265201 , 1939 ;

With ammonia

T=280°C; P=169167 Torr; Hydrogenation.an einen Bariumoxid-Kupferoxid-Chromoxid-Katalysator;

Full Text Show Details

I.G. Farbenind.

Patent: DE695472 , 1938 ; DRP/DRBP Org.Chem. Full Text Show Details

394

Synthesize Find similar

Rx-ID: 5403471 Find similar reactions

Synthesize Find similar

Synthesize Find similar

Synthesize Find similar

Gen. Aniline and Film Corp.

Patent: US2265201 , 1939 ;

T=150 - 250°C; P=147102 Torr; Hydrogenation;

Full Text Show Details

I.G. Farbenind.

Patent: DE695472 , 1938 ; DRP/DRBP Org.Chem. Full Text Show Details

395

Synthesize Find similar

T=250°C; P=147102 Torr; Hydrogenation;

Synthesize Find similar

Rx-ID: 5403472 Find similar reactions

Gen. Aniline and Film Corp.

Patent: US2265201 , 1939 ; Full Text Show Details


396

Synthesize Find similar T=280°C; P=169167 Torr; Hydrogenation;

Synthesize Find similar

Rx-ID: 5403473 Find similar reactions

Gen. Aniline and Film Corp.

Patent: US2265201 , 1939 ; Full Text Show Details


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