Hydrochloric Acid → HCID 21568344, compound
Reaction equation
[ClH:1].O[C:3]([CH:16]1[CH2:21][CH2:20][N:19]([CH2:22][CH2:23][CH2:24][C:25]([C:27]2[CH:36]=[CH:35][C:34]3[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=3)[CH:28]=2)=[O:26])[CH2:18][CH2:17]1)([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.Cl>C(O)(C)C>[ClH:1].[C:10]1([C:3]([C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)=[C:16]2[CH2:17][CH2:18][N:19]([CH2:22][CH2:23][CH2:24][C:25]([C:27]3[CH:36]=[CH:35][C:34]4[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=4)[CH:28]=3)=[O:26])[CH2:20][CH2:21]2)[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 17.6 g (0.038 mole) of 4-[4-(α-hydroxy-α-phenylbenzyl)piperidino]-1-(2-naphthyl)butan-1-one hydrochloride, 400 ml of concentrated HCl and 1500 ml of isopropyl alcohol is heated on a steam bath for 16 hours after which the solvent and excess acid are removed at reduced pressure. The remaining residue is recrystallized from isopropyl alcohol and ethyl acetate to give 4-[4-(diphenylmethylene)piperidino]-1-(2-naphthyl)butan-1-one hydrochloride.
Workup
- temperatureis heated on a steam bath for 16 hours after which the solvent and excess acid
- customare removed at reduced pressure
- customThe remaining residue is recrystallized from isopropyl alcohol and ethyl acetate
Sources & evidence
- ORD record
- ord-8dfbb2e2429d4ccbb42b7483ad2471f3
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03931197
Reaction notes
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