반응식
[Cl:1][C:2]1[C:3]2[CH:12]=[CH:11][CH:10]=[CH:9][C:4]=2[S:5][C:6]=1[CH:7]=O.[CH3:13][O:14][C:15](=[O:36])[CH:16]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C([O-])(O)=O.[Na+]>C1(C)C=CC=CC=1>[CH3:13][O:14][C:15](=[O:36])/[CH:16]=[CH:7]/[C:6]1[S:5][C:4]2[CH:9]=[CH:10][CH:11]=[CH:12][C:3]=2[C:2]=1[Cl:1]참가 물질
5
실험 절차
A solution of 3.52 g (18.3 mmol) of 13 in 50 mL toluene was treated with methyl(triphenylphosphoranylidene)acetate (7.48 g, 21.9 mmol). After 4 h, saturated NaHCO3 solution (50 mL) was added and the mixture extracted with ethyl acetate (2×75 mL). The combined ethyl acetate solution was washed with brine (50 mL), dried (Na2SO4), filtered and evaporated. Purification by flash chromatography on silica gel (5% ethyl acetate/hexane) provided 3.60 g (14.6 mmol, 80%) of the enoate (14).
후처리
- extractionthe mixture extracted with ethyl acetate (2×75 mL)
- washThe combined ethyl acetate solution was washed with brine (50 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- customevaporated
- customPurification by flash chromatography on silica gel (5% ethyl acetate/hexane)
출처 및 근거
- ORD 기록
- ord-824feff9e81248b8b464da03e37175b7
- 출처 데이터셋
- uspto-grants-2014_06
- 특허 번호
- US08754122B2
연결된 노트
불러오는 중…