Acetic Acid → 4-Anilinopiperidine

HRID 1948980Notes

Reaction equation

HRID 1948980 reaction equation
O.Cl.[NH:3]1[CH2:8][CH2:7][C:6](=O)[CH2:5][CH2:4]1.[NH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(O)(=O)C>[Zn].O>[NH:10]([CH:6]1[CH2:7][CH2:8][NH:3][CH2:4][CH2:5]1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Participants

6

Reactant 3

HCID 176Acetic AcidHCID 6115AnilineHCID 2723901Piperonylamine

Product 1

HCID 899824-Anilinopiperidine

Reagents, catalysts & solvents 2

HCID 23994ZincCatalystHCID 962WaterSolvent

Conditions

Temperature
60 °C

Procedure

In a three neck round bottom flask equipped with mechanical stirrer and water condenser, 15.36 gm (o.10 moles) of 4-piperidone hydrochloride monohydrate and 9.3 gm (0.10 moles) of aniline were added. To this mixture, 6.5 gm (0.10 moles) of zinc and 0.6 gm (0.10 moles) of 90% acetic acid were added. The reaction mixture was stirred at room temperature for 24 hrs and at 50 to 70° C. for 24 hrs. Water was then added to the reaction mixture and filtered. Crushed ice was added to the filtrate and was neutralized with excess of aqueous sodium hydroxide solution. The crude 4-anilinopiperidine was obtained by filtration.

Workup

  1. customIn a three neck round bottom flask equipped with mechanical stirrer and water condenser
  2. filtrationfiltered
  3. additionCrushed ice was added to the filtrate

Sources & evidence

ORD record
ord-28205c74abd14c16b9e1b4c8ce420d5e
Source dataset
uspto-grants-2013_03
Patent number
US08399677B2

Reaction notes

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