Potassium Iodide → 4-(p-bromophenyl)-4-hydroxy-N,N-dimethyl-alpha,alpha-diphenylpiperidine-1-butyramide hydrate
반응식
[Br-].[CH3:2][N+:3]([CH3:21])=[C:4]1[C:8]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH2:7][CH2:6][O:5]1.Cl.[Br:23][C:24]1[CH:29]=[CH:28][C:27]([C:30]2([OH:36])[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]2)=[CH:26][CH:25]=1.C(=O)([O-])[O-].[Na+].[Na+].[I-].[K+]>O.CC(C)CC(=O)C>[OH2:5].[Br:23][C:24]1[CH:29]=[CH:28][C:27]([C:30]2([OH:36])[CH2:31][CH2:32][N:33]([CH2:6][CH2:7][C:8]([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=3)([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[C:4]([N:3]([CH3:21])[CH3:2])=[O:5])[CH2:34][CH2:35]2)=[CH:26][CH:25]=1참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
A mixture of 12.1 parts of dimethyl (tetrahydro-3,3-diphenyl-2-furylidene) ammonium bromide, 8.8 parts of 4-(p-bromophenyl)-4-piperidinol hydrochloride, 10.6 parts of sodium carbonate, 0.5 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 14 hours with water separator. The reaction mixture is cooled and water (200 parts) is added. The organic layer is separated, washed with diluted sodium hydroxide solution, dried, filtered, and while stirring the filtrate, the product is crystallized. It is filtered off and recrystallized from 80 parts of 4-methyl-2-pentanone (activated charcoal), yielding 4-(p-bromophenyl)-4-hydroxy-N,N-dimethyl-α,α-diphenylpiperidine-1-butyramide hydrate; m.p. 123.7° C.
후처리
- temperatureThe reaction mixture is cooled
- customThe organic layer is separated
- washwashed with diluted sodium hydroxide solution
- customdried
- filtrationfiltered
- stirringwhile stirring the filtrate
- customthe product is crystallized
- filtrationIt is filtered off
- customrecrystallized from 80 parts of 4-methyl-2-pentanone (activated charcoal)
출처 및 근거
- ORD 기록
- ord-49d8828a0da143bd8ce8f5b9afa09162
- 출처 데이터셋
- uspto-grants-1998_08
- 특허 번호
- US05798093
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