Hydrochloric Acid → HCID 20288060, compound
Reaction equation
C([N:4]1[CH2:9][CH2:8][CH:7]([CH2:10][C:11]([C:13]2[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=2)=[O:12])[CH2:6][CH2:5]1)(=O)C.[ClH:21]>>[ClH:21].[CH3:20][O:19][C:16]1[CH:17]=[CH:18][C:13]([C:11](=[O:12])[CH2:10][CH:7]2[CH2:6][CH2:5][NH:4][CH2:9][CH2:8]2)=[CH:14][CH:15]=1Participants
3
Conditions
- Temperature
- 100 °C
Procedure
A mixture of 10 parts of 1-acetyl-4-[2-(4-methoxyphenyl)-2-oxoethyl]piperidine and 50 parts of a hydrochloric acid solution 6 N is stirred and heated for 4 hours at 100° C. The reaction mixture is allowed to cool to room temperature. The precipitated product is filtered off and crystallized from 2-propanol, yielding 5.8 parts (59%) of 1-(4-methoxyphenyl)-2-(4-piperidinyl)ethanone hydrochloride; mp. 250.7° C.
Workup
- temperatureto cool to room temperature
- filtrationThe precipitated product is filtered off
- customcrystallized from 2-propanol
Sources & evidence
- ORD record
- ord-f834473bed7e446cbf91ca0d20b20a1a
- Source dataset
- uspto-grants-1981_03
- Patent number
- US04254127
Reaction notes
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