ethyl (2Z)-3-(pyridin-4-yl)but-2-enoate → Ethyl 3-(pyridin-4-yl)butanoate
반응식
[N:1]1[CH:6]=[CH:5][C:4](/[C:7](/[CH3:14])=[CH:8]\[C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:3][CH:2]=1>[Pd].CCO>[N:1]1[CH:6]=[CH:5][C:4]([CH:7]([CH3:14])[CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:3][CH:2]=1참가 물질
4
실험 절차
Palladium on carbon (70 mg, 10 wt. %) was added to a solution of (Z)-ethyl 3-(pyridin-4-yl)but-2-enoate (0.70 g, 3.66 mmol) in EtOH (10 ml) and hydrogenated under balloon pressure for 18 h. The reaction mixture was filtered through a pad of celite and washed with EtOH. The filtrate was concentrated under reduced pressure to afford 0.50 g (71.4%) of ethyl 3-(pyridin-4-yl)butanoate as light brown color liquid.
후처리
- filtrationThe reaction mixture was filtered through a pad of celite
- washwashed with EtOH
- concentrationThe filtrate was concentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-e3eea5b8af234a3ab04fcbb65a93dd10
- 출처 데이터셋
- uspto-grants-2015_06
- 특허 번호
- US09067888B2
반응 노트
불러오는 중…