Sodium cyanoborohydride → t-Butyl 7-phenyl-3,5-dihydroxy-6-heptenoate
반응식
[C:1]1([CH:7]=[CH:8][CH:9]([OH:21])[CH2:10][C:11](=[O:20])[CH2:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([BH3-])#N.[Na+]>CC(C)[O-].CC(C)[O-].CC(C)[O-].[Cl-].[Ti+4]>[C:1]1([CH:7]=[CH:8][CH:9]([OH:21])[CH2:10][CH:11]([OH:20])[CH2:12][C:13]([O:15][C:16]([CH3:17])([CH3:18])[CH3:19])=[O:14])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1참가 물질
4
실험 절차
By carrying out the reaction as in Example 9 but starting from 1.0 g of t-butyl 7-phenyl-5-hydroxy-3-oxo-6-heptenoate (3.42 mmol) and using 0.95 cm3 of titanium chloride triisopropoxide (3.77 mmol) and 261.8 mg of sodium cyanoborohydride (3.95 mmol), there is obtained, after reacting for 3 hours 10 minutes, with a yield of 55%, 550 mg of t-butyl 7-phenyl-3,5-dihydroxy-6-heptenoate for which the syn/anti ratio is equal to 90/10.
후처리
- customthe reaction as in Example 9
- customthere is obtained
출처 및 근거
- ORD 기록
- ord-6c3857cf6e2f495d9d57da5b36dda2b2
- 출처 데이터셋
- uspto-grants-1994_09
- 특허 번호
- US05347039
반응 노트
불러오는 중…