Potassium Carbonate → Trans-1-(4-fluorophenyl)-3-(3-hydroxy-4-phenoxy-1-pyrrolidinyl)-1-propanone
반응식
[O:1]([CH:8]1[CH2:12][NH:11][CH2:10][CH:9]1[OH:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.CN(C)[CH2:17][CH2:18][C:19]([C:21]1[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=1)=[O:20].C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[F:27][C:24]1[CH:23]=[CH:22][C:21]([C:19](=[O:20])[CH2:18][CH2:17][N:11]2[CH2:12][C@@H:8]([O:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[C@H:9]([OH:13])[CH2:10]2)=[CH:26][CH:25]=1참가 물질
반응 조건
- 온도
- 70 °C
실험 절차
A mixture of 3.6 g. (0.02 mole) of 4-phenoxy-3-pyrrolidinol, 5 g. (0.0215 mole) of β-dimethylamino-p-fluoropropiophenone hydrochloride, 10 g. of potassium carbonate and 50 ml. of dimethylformamide was heated with stirring at 70° C. for 6 hr. while nitrogen gas was bubbled through the reaction mixture. The mixture was poured into water and extracted twice with benzene. The combined extracts were dried over anhydrous sodium sulfate and concentrated to give 6.1 g. of an oil as residue. The oil was chromatographed on 130 g. of silica gel. The desired compound was eluted with 20% acetone in benzene and 2.6 g. (39%) of an oil which gradually crystallized upon standing was obtained. This solid was recrystallized from petroleum ether diethylether to yield a white solid, m.p. 77°-80° C.
후처리
- additionA mixture of 3.6 g
- customwhile nitrogen gas was bubbled through the reaction mixture
- additionThe mixture was poured into water
- extractionextracted twice with benzene
- dry with materialThe combined extracts were dried over anhydrous sodium sulfate
- concentrationconcentrated
- customto give 6.1 g
- customThe oil was chromatographed on 130 g
- washThe desired compound was eluted with 20% acetone in benzene and 2.6 g
- custom(39%) of an oil which gradually crystallized
- customupon standing was obtained
- customThis solid was recrystallized from petroleum ether diethylether
- customto yield a white solid, m.p. 77°-80° C.
출처 및 근거
- ORD 기록
- ord-9a48fba82529470a83c5cd69370247b0
- 출처 데이터셋
- uspto-grants-1986_04
- 특허 번호
- US04585785
반응 노트
불러오는 중…