Ethyl chloroformate → 4-(p-FLUOROBENZOYL)-4-HYDROXYPIPERIDINE HYDROCHLORIDE
반응식
C([O:4][C:5]1([C:12](=[O:20])[C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][CH:14]=2)[CH2:10][CH2:9][N:8](C)[CH2:7][CH2:6]1)(=O)C.[Cl:21]C(OCC)=O>C1C=CC=CC=1>[ClH:21].[F:19][C:16]1[CH:17]=[CH:18][C:13]([C:12]([C:5]2([OH:4])[CH2:10][CH2:9][NH:8][CH2:7][CH2:6]2)=[O:20])=[CH:14][CH:15]=1참가 물질
4
실험 절차
To 27.9 grams (0.1 mole) of 4-acetoxy-4-(p-fluorobenzoyl)-1-methylpiperidine in 200 ml. of benzene was added 27.1 (0.25 mole) of ethyl chloroformate. The mixture was refluxed for 48 hours. The mixture was extracted with H2O, the organic solution was dried (MgSO4) and filtered. The filtrate was concentrated. To the resulting oil was added 250 ml. of 6 Normal HCl and the mixture was refluxed for seventy-two hours. Most of the water was removed under reduced pressure. Ethanol was added and the solution cooled. The solid which precipitated was collected by filtration and recrystallized from ethanol giving eighteen grams of 4-(p-fluorobenzoyl)-4-hydroxypiperidine hydrochloride. Melting point 241°-243° C.
후처리
- temperatureThe mixture was refluxed for 48 hours
- extractionThe mixture was extracted with H2O
- dry with materialthe organic solution was dried (MgSO4)
- filtrationfiltered
- concentrationThe filtrate was concentrated
- additionTo the resulting oil was added 250 ml
- temperatureof 6 Normal HCl and the mixture was refluxed for seventy-two hours
- customMost of the water was removed under reduced pressure
- additionEthanol was added
- temperaturethe solution cooled
- customThe solid which precipitated
- filtrationwas collected by filtration
- customrecrystallized from ethanol giving eighteen grams of 4-(p-fluorobenzoyl)-4-hydroxypiperidine hydrochloride
출처 및 근거
- ORD 기록
- ord-6c5d9db3dbc44eb38243c8bfa9e9174d
- 출처 데이터셋
- uspto-grants-1977_05
- 특허 번호
- US04021564
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