2-Bromoethyl ethyl ether → 1-(2-Ethoxyethyl)-4-cyano-4-phenyl-piperidine
반응식
[C:1]([C:3]1([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH2:8][CH2:7][NH:6][CH2:5][CH2:4]1)#[N:2].[CH2:15]([O:17][CH2:18][CH2:19]Br)[CH3:16]>>[CH2:15]([O:17][CH2:18][CH2:19][N:6]1[CH2:5][CH2:4][C:3]([C:1]#[N:2])([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH2:8][CH2:7]1)[CH3:16]참가 물질
3
실험 절차
The title compound was prepared as described in Example I 2 from 4-cyano-4-phenylpiperidine and 2-bromoethyl ethyl ether excluding KI: Reaction time under reflux 6 hours. The compound boiled at 130°-135°/0.005 mm Hg.
후처리
- customReaction time
- temperatureunder reflux 6 hours
출처 및 근거
- ORD 기록
- ord-ce9dad50c54a49b78ff270fedfd9f16e
- 출처 데이터셋
- uspto-grants-1993_07
- 특허 번호
- US05227389
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