Sodium Hydroxide → 4-(3-(1-Methylethoxy)phenyl)-1-piperidinecarboxylic acid phenyl ester
반응식
C([N:3]1[CH2:8][CH2:7][CH:6]([C:9]2[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH:16]([CH3:18])[CH3:17])[CH:10]=2)[CH2:5][CH2:4]1)C.Cl[C:20]([O:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)=[O:21].[OH-].[Na+]>C1(C)C=CC=CC=1>[C:23]1([O:22][C:20]([N:3]2[CH2:8][CH2:7][CH:6]([C:9]3[CH:14]=[CH:13][CH:12]=[C:11]([O:15][CH:16]([CH3:18])[CH3:17])[CH:10]=3)[CH2:5][CH2:4]2)=[O:21])[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1참가 물질
반응 조건
- 온도
- 45 °C
실험 절차
To N-ethyl-4-(3-(1-methylethoxy)phenyl)piperidine (Preparation 45, 2.0 g, 8.10 mmol) in toluene (20 ml) at 85° C. was added phenyl chloroformate (1.0 ml, 9.70 mmol) and the mixture was heated at reflux for 4 h. The solution was cooled to 45° C. and aqueous sodium hydroxide solution (1 ml of 50% aqueous sodium hydroxide solution in 8 ml of water) was added. The reaction mixture was cooled to room temperature and the organic layer was separated and washed with methanol: 1N aqueous hydrochloric acid (1:1, 2×20 ml), methanol: 1N aqueous sodium hydroxide solution (1:1, 25 ml) and water (20 ml). The organic extract was dried (MgSO4), filtered and concentrated in vacuo to give the crude product. This was purified by silica column chromatography eluting with ethyl acetate:hexane (1:5) to give the title compound as an oil (1.7 g, 62%).
후처리
- temperaturethe mixture was heated
- temperatureat reflux for 4 h
- temperatureThe reaction mixture was cooled to room temperature
- customthe organic layer was separated
- washwashed with methanol
- extractionThe organic extract
- dry with materialwas dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto give the crude product
- customThis was purified by silica column chromatography
- washeluting with ethyl acetate:hexane (1:5)
출처 및 근거
- ORD 기록
- ord-55fc36ca6aa6455d98b4508a4be3a999
- 출처 데이터셋
- uspto-grants-2003_08
- 특허 번호
- US06610711B2
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