Hydrochloric Acid → HCID 20030105, compound

HRID 638004Notes

Reaction equation

HRID 638004 reaction equation
[C:1]([CH2:3][N:4]1[CH2:9][CH2:8][CH:7]([C:10](=[O:18])[C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[CH2:6][CH2:5]1)#[N:2].[ClH:19].[H][H]>C(O)(=O)C.[Pt]=O>[ClH:19].[NH2:2][CH2:1][CH2:3][N:4]1[CH2:5][CH2:6][CH:7]([C:10](=[O:18])[C:11]2[CH:12]=[CH:13][C:14]([F:17])=[CH:15][CH:16]=2)[CH2:8][CH2:9]1

Participants

6

Procedure

14.1 g (0.05 mol) of N-(cyanomethyl)-4-(p-fluorobenzoyl)-piperidine are dissolved in 1.5 liters of glacial acetic acid and 30 ml of concentrated hydrochloric acid and hydrogenated together with 2 g of platinum oxide in a hydrogen atmosphere. After 6 hours, the theoretical amount of 2.25 liters of hydrogen is absorbed. The catalyst is then filtered off with suction and the filtrate is concentrated to approximately 30 ml in a water-jet vacuum. There is added to the resulting crystal mass 5 ml of isopropanol and 15 ml of ether and filtration with suction is carried out. After filtration with suction and drying, N-(2-aminoethyl)-4-(p-fluorobenzoyl)-piperidine hydrochloride is obtained which, after recrystallisation from methanol, melts at 265° with decomposition.

Workup

  1. customthe theoretical amount of 2.25 liters of hydrogen is absorbed
  2. filtrationThe catalyst is then filtered off with suction
  3. concentrationthe filtrate is concentrated to approximately 30 ml in a water-jet vacuum
  4. additionThere is added to the resulting crystal mass 5 ml of isopropanol and 15 ml of ether and filtration with suction
  5. filtrationAfter filtration with suction
  6. customdrying

Sources & evidence

ORD record
ord-d88d9fd90de44b5fae36cb4b229aa33d
Source dataset
uspto-grants-1985_12
Patent number
US04559349

Reaction notes

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