Hydrochloric Acid → 1-[(Diphenylmethoxy)acetyl]-3-phenylpiperidine
반응식
[C:1]1([CH:7]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[O:8][CH2:9][C:10](Cl)=[O:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:19]1([CH:25]2[CH2:30][CH2:29][CH2:28][NH:27][CH2:26]2)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C(N(CC)CC)C.Cl>C(Cl)Cl.O>[C:1]1([CH:7]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[O:8][CH2:9][C:10]([N:27]2[CH2:28][CH2:29][CH2:30][CH:25]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:26]2)=[O:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1참가 물질
실험 절차
A solution of 4.5 g (17.2 mmole) of (diphenylmethoxy) acetyl chloride in 50 cm3 of methylene chloride was added drop-wise at room temperature to a solution of 2.8 g (17.2 mmole) of 3-phenylpiperidine [prepared according to M. Julia et al., Bull. Soc. Chim. Fr. 1968, 987] and 3.5 g (34.4 mmole) of triethylamine in 100 cm3 of methylene chloride. The reaction mixture was heated to reflux for 4 hours; it was allowed to stand overnight and was then poured into a solution of 10 cm3 of concentrated hydrochloric acid in 300 cm3 of water. The mixture was extracted with methylene chloride, washed with water and dried on sodium sulfate. After the solvent was evaporated under reduced pressure, the residue was purified by silica gel filtration (eluent, hexaneethyl acetate, 1/1), then by recrystallization from a hexane-ethyl acetate mixture. There was obtained 4.3 g (yield: 65%) of 1-[(diphenylmethoxy)acetyl]-3-phenylpiperidine.
후처리
- temperatureThe reaction mixture was heated
- temperatureto reflux for 4 hours
- extractionThe mixture was extracted with methylene chloride
- washwashed with water
- customdried on sodium sulfate
- customAfter the solvent was evaporated under reduced pressure
- filtrationthe residue was purified by silica gel filtration (eluent, hexaneethyl acetate, 1/1)
- customby recrystallization from a hexane-ethyl acetate mixture
출처 및 근거
- ORD 기록
- ord-93aaf05872ae490a9d9e9749bfb780d3
- 출처 데이터셋
- uspto-grants-1990_09
- 특허 번호
- US04957927
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