반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([OH:12])[C:9]#[C:10][CH3:11])=[CH:4][CH:3]=1>[Pd].CC([O-])=O.CC([O-])=O.[Pb+2]>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([OH:12])/[CH:9]=[CH:10]\[CH3:11])=[CH:6][CH:7]=1참가 물질
3
실험 절차
Under nitrogen, hydrogenate a mixture of 10 g (0.055 mole) of 1-(4-chlorophenyl)-2-butyn-1-ol and 0.6 g Lindlar catalyst. Following the reaction via NMR the reaction is complete in about two days. The hydrogenation is stopped and the reaction stirred under N2 at room temperature overnight. Filter off the catalysts, wash with methylene chloride combine the filtrate and evaporate to yield the title compound.
후처리
- customthe reaction via NMR the reaction
- filtrationFilter off the catalysts
- washwash with methylene chloride
- customevaporate
출처 및 근거
- ORD 기록
- ord-93abc6b367ac4c85828867dcc8b49366
- 출처 데이터셋
- uspto-grants-1987_08
- 특허 번호
- US04689341
연결된 노트
불러오는 중…