반응식
[CH3:1][N:2]1CCCC1=O.[CH3:8][O:9][C:10]1[CH:25]=[CH:24][C:13]2[S:14][C:15]3[CH:22]=[CH:21][CH:20]=[C:19](Cl)[C:16]=3[CH2:17][CH2:18][C:12]=2[CH:11]=1.[Cu](C#N)C#N.O.N>S([O-])([O-])(=O)=O.[Cu+2].C1C=CC=CC=1.O>[CH3:8][O:9][C:10]1[CH:25]=[CH:24][C:13]2[S:14][C:15]3[CH:22]=[CH:21][CH:20]=[C:19]([C:1]#[N:2])[C:16]=3[CH2:17][CH2:18][C:12]=2[CH:11]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
실험 절차
To 100 ml of N-methylpyrrolidone was added 10.8g of 2-methoxy-9-chloro-10,11-dihydrodibenzo[b,f]thiepin, 10.7g of copper cyanide and 0.4g of anhydrous copper sulfate and the resulting mixture was stirred at 190°-195° C for 15 hours. After cooling, to the mixture was added 28% ammonia water, 200 ml of water and 200 ml of benzene and the resulting mixture was shaked and filtered with celite. The filtrate was extracted with benzene. The extract was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate and freed of the solvent to obtain 9.0g of light brown cyrstals. This product was chromatographed over silica gel and eluted with benzene, there was obtained 5.4g (50%) of 2-methoxy-9-cyano-10,11-dihydrodibenzo[ b,f]thiepin as colorless prismatic crystals having a melting point of 129°-130° C.
후처리
- temperatureAfter cooling, to the mixture
- filtrationfiltered with celite
- extractionThe filtrate was extracted with benzene
- washThe extract was washed with saturated sodium chloride solution
- dry with materialdried over anhydrous sodium sulfate
- customto obtain 9.0g of light brown cyrstals
- customThis product was chromatographed over silica gel
- washeluted with benzene
출처 및 근거
- ORD 기록
- ord-4700ad0dff764d38b8e5dd48ae4e6200
- 출처 데이터셋
- uspto-grants-1978_07
- 특허 번호
- US04101667
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