반응식
[C:1]([O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)(=[O:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][C:9](O)=[O:10].[BH4-].[Na+].[H][H].[B-](F)(F)(F)[O+](C)C>O1CCCC1.O>[OH:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][C:1]([O:13][CH2:14][C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)=[O:12]참가 물질
실험 절차
The product from 11a (12.9 g; 46.3 mmol) was added in portions to a stirred mixture of sodium borohydride (1.70 g; 45.0 mmol) in dry tetrahydrofuran (25 mL). After the evolution of hydrogen subsided, a solution of boron trifluoride dimethyl etherate (4.6 mL; 5.7 g; 50 mmol) in dry tetrahydrofuran (15 mL) was added drop-wise. The exothermic reaction was moderated with a cold water bath. After stirring 4 h at ambient temperature, the reaction mixture was hydrolyzed with cold water (20 mL). The mixture was separated and the organic phase was evaporated; the residue was mixed with water (20 mL) and dichloromethane (70 mL) to give an emulsion that separated on standing overnight. The organic layer was washed with water (4×15 mL) until the washings were neutral to pH paper. Following drying (Na2SO4), filtration, and evaporation 11.95 g (98%) product was obtained (oil).
후처리
- customThe exothermic reaction
- customwas moderated with a cold water bath
- customThe mixture was separated
- customthe organic phase was evaporated
- additionthe residue was mixed with water (20 mL) and dichloromethane (70 mL)
- customto give an emulsion that
- customseparated
- waiton standing overnight
- washThe organic layer was washed with water (4×15 mL) until the washings
- customFollowing drying
- filtration(Na2SO4), filtration
- customevaporation 11.95 g (98%) product
- customwas obtained (oil)
출처 및 근거
- ORD 기록
- ord-b66c3eb0870f4433b3c405259ff9572b
- 출처 데이터셋
- uspto-grants-2016_02
- 특허 번호
- US09249086B2
연결된 노트
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