반응식
[CH3:1][N:2]([CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][C:5]1=O)[CH3:3].Cl.[CH3:12][O:13][C:14]1[CH:15]=[C:16]([NH:20]N)[CH:17]=[CH:18][CH:19]=1.Cl>C(O)C>[CH3:1][N:2]([CH3:3])[CH:4]1[CH2:9][C:8]2[C:17]3[C:16](=[CH:15][C:14]([O:13][CH3:12])=[CH:19][CH:18]=3)[NH:20][C:7]=2[CH2:6][CH2:5]1참가 물질
실험 절차
A solution of 7 g. of dimethylaminocyclohexanone and 8.4 g. of 3-methoxyphenylhydrazine hydrochloride in 40 ml. of absolute ethyl alcohol and 12 ml. of 4-N hydrogen chloride in ethyl alcohol was heated under reflux for two hours. The reaction mixture was allowed to stand for sixteen hours, filtered, and the filtrate was evaporated to dryness under reduced pressure. The residue was taken up in water, made alkaline with dilute sodium hydroxide and extracted with ether. The ether extract was washed with water, dried, ethereal hydrogen chloride was added, and the resulting oily precipitate was collected by decantation, recrystallized twice from isopropyl alcohol, suspended in chloroform and treated with dilute sodium hydroxide. The chloroform extract was evaporated to dryness under reduced pressure to give 3-(dimethylamino)-7-methoxy-1,2,3,4-tetrahydrocarbazole, m.p. 100°-105° C.
후처리
- temperatureunder reflux for two hours
- waitto stand for sixteen hours
- filtrationfiltered
- customthe filtrate was evaporated to dryness under reduced pressure
- extractionextracted with ether
- extractionThe ether extract
- washwas washed with water
- customdried
- additionethereal hydrogen chloride was added
- customthe resulting oily precipitate was collected by decantation
- customrecrystallized twice from isopropyl alcohol
- additiontreated with dilute sodium hydroxide
- extractionThe chloroform extract
- customwas evaporated to dryness under reduced pressure
출처 및 근거
- ORD 기록
- ord-0e08576729e94ed486fc6f1c4f71f701
- 출처 데이터셋
- uspto-grants-1981_03
- 특허 번호
- US04257952
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