Hydrochloric Acid → HCID 20343991, compound
Reaction equation
[C:1]([C:4]1([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[S:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:9][CH2:8][N:7](C#N)[CH2:6][CH2:5]1)(=[O:3])[CH3:2].[ClH:25]>>[ClH:25].[C:1]([C:4]1([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[S:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1)(=[O:3])[CH3:2]Participants
3
Procedure
A solution of 4.8 g of 4-acetyl-1-cyano-4-(2-phenylthiophenyl)piperidine, Example 8, in 50 ml of 2 N hydrochloric acid is refluxed for 16 hours, effecting a white precipitate. The precipitate is collected by filtration and then washed twice with 50 ml portions of water and dried, providing 4-acetyl-4-(2-phenylthiophenyl)piperidine hydrochloride.
Workup
- filtrationThe precipitate is collected by filtration
- washwashed twice with 50 ml portions of water
- customdried
Sources & evidence
- ORD record
- ord-932ba553594a489fa8a57de8c6430ddf
- Source dataset
- uspto-grants-1980_04
- Patent number
- US04198419
Reaction notes
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