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6 reactions in Reaxys
2016-02-19 01h:13m:03s (EST)
6 reactions in Reaxys
2016-02-19 01h:19m:56s (EST)
HN
1. Query
Search as: As drawn 2. Query
(1. Query) AND itemno in (1)
Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.
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2016-02-19 01:23:44
H N
N
Rx-ID: 158565 View in Reaxys 1/6 Yield
Conditions & References With palladium on activated charcoal, ethanol, T= 100 °C , p= 73550.8Torr , Hydrogenation Sury; Hoffmann; Helvetica Chimica Acta; vol. 37; (1954); p. 2133,2141; Helvetica Chimica Acta; vol. 38; (1955); p. 728,735 View in Reaxys Patent; CIBA; US2820038; (1954) View in Reaxys With acetic acid, platinum, T= 40 °C , Hydrogenation Sury; Hoffmann; Helvetica Chimica Acta; vol. 37; (1954); p. 2133,2141; Helvetica Chimica Acta; vol. 38; (1955); p. 728,735 View in Reaxys Patent; CIBA; US2820038; (1954) View in Reaxys
O N H N
Rx-ID: 482539 View in Reaxys 2/6 Yield
Conditions & References With ethanol, nickel, T= 100 °C , p= 73550.8Torr , Hydrogenation Sury; Hoffmann; Helvetica Chimica Acta; vol. 38; (1955); p. 728,733 View in Reaxys
(+-)-diphenyl-<2>piperidyl-methanol
H N
Rx-ID: 5488731 View in Reaxys 3/6 Yield
Conditions & References With pentan-1-ol, sodium Sury; Hoffmann; Helvetica Chimica Acta; vol. 38; (1955); p. 728,733 View in Reaxys With sodium, butan-1-ol Sury; Hoffmann; Helvetica Chimica Acta; vol. 38; (1955); p. 728,733 View in Reaxys
Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.
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Cl
O
H N
Rx-ID: 22212125 View in Reaxys 4/6 Yield
Conditions & References Reaction Steps: 2 2: nickel catalyst; ethanol / 100 °C / 73550.8 Torr / Hydrogenation With ethanol, nickel Sury; Hoffmann; Helvetica Chimica Acta; vol. 38; (1955); p. 728,733 View in Reaxys
N
H N
Rx-ID: 22218665 View in Reaxys 5/6 Yield
Conditions & References Reaction Steps: 3 1: NaNH2; dioxane / anschliessendes Erhitzen mit 2-Brom-pyridin 2: aqueous methanol. KOH-solution / 220 °C 3: platinum; acetic acid / 40 °C / Hydrogenation With 1,4-dioxane, potassium hydroxide, sodium amide, acetic acid, platinum Sury; Hoffmann; Helvetica Chimica Acta; vol. 37; (1954); p. 2133,2141; Helvetica Chimica Acta; vol. 38; (1955); p. 728,735 View in Reaxys
H N
N N
Rx-ID: 22221035 View in Reaxys 6/6 Yield
Conditions & References Reaction Steps: 2 1: aqueous methanol. KOH-solution / 220 °C 2: platinum; acetic acid / 40 °C / Hydrogenation With potassium hydroxide, acetic acid, platinum Sury; Hoffmann; Helvetica Chimica Acta; vol. 37; (1954); p. 2133,2141; Helvetica Chimica Acta; vol. 38; (1955); p. 728,735 View in Reaxys
Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.
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