Water → 79601-34-6
반응식
Br.[CH2:2]([N:5]1[CH2:10][CH2:9][CH2:8][CH:7]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([OH:17])[CH:12]=2)[CH2:6]1)[CH2:3][CH3:4].CC(C)([O-])C.[K+].[CH2:24]([Cl:31])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.O>C(O)(C)(C)C>[ClH:31].[CH2:2]([N:5]1[CH2:10][CH2:9][CH2:8][CH:7]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[CH:12]=2)[CH2:6]1)[CH2:3][CH3:4]참가 물질
6
실험 절차
A mixture of N-n-propyl-3-(3-hydroxyphenyl)piperidine hydrobromide (1.0 g, 0.0033 mol), potassium t-butoxide (1.0 g, 0.009 mol) and benzylchloride (1.0 g, 0.009 mol) in t-butanol (25 ml) was refluxed for 1 h. Water was added and the mixture extracted with ether. The organic phase was dried with Na2SO4 and evaporated to dryness giving a pale yellow oily residue. The residue was chromatographed through a silica gel column with methanol as eluant. The pertinent fractions were collected and evaporated to dryness. The oily residue was dissolved in ether and HCl-saturated ether was added, giving white crystals. Evaporation and treatment of the residue with acetone gave 0.60 g (52%) of the desired product as white crystals, mp. 171° C.
후처리
- temperaturewas refluxed for 1 h
- extractionthe mixture extracted with ether
- dry with materialThe organic phase was dried with Na2SO4
- customevaporated to dryness
- customgiving a pale yellow oily residue
- customThe residue was chromatographed through a silica gel column with methanol as eluant
- customThe pertinent fractions were collected
- customevaporated to dryness
- dissolutionThe oily residue was dissolved in ether
- additionHCl-saturated ether was added
- customgiving white crystals
- customEvaporation and treatment of the residue with acetone
출처 및 근거
- ORD 기록
- ord-a21490e1367e4ff5b3f1e0f2889c2fd2
- 출처 데이터셋
- uspto-grants-1984_01
- 특허 번호
- US04426386
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