Hydrochloric Acid → HCID 20030105, compound
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]1Participants
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
- customthe theoretical amount of 2.25 liters of hydrogen is absorbed
- filtrationThe catalyst is then filtered off with suction
- concentrationthe filtrate is concentrated to approximately 30 ml in a water-jet vacuum
- additionThere is added to the resulting crystal mass 5 ml of isopropanol and 15 ml of ether and filtration with suction
- filtrationAfter filtration with suction
- customdrying
Sources & evidence
- ORD record
- ord-d88d9fd90de44b5fae36cb4b229aa33d
- Source dataset
- uspto-grants-1985_12
- Patent number
- US04559349
Reaction notes
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