Citric Acid → (RS)-4-t-butyldimethylsilyloxy-3-methyl-2-(2,2,2-trifluoroethyl)cyclopent-2-en-1-one
반응식
[OH:1][CH:2]1[CH2:6][C:5](=[O:7])[C:4]([CH2:8][C:9]([F:12])([F:11])[F:10])=[C:3]1[CH3:13].N1C=CN=C1.[C:19]([Si:23]([CH3:26])([CH3:25])Cl)([CH3:22])([CH3:21])[CH3:20].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CN(C)C=O>[Si:23]([O:1][CH:2]1[CH2:6][C:5](=[O:7])[C:4]([CH2:8][C:9]([F:10])([F:11])[F:12])=[C:3]1[CH3:13])([C:19]([CH3:22])([CH3:21])[CH3:20])([CH3:26])[CH3:25]참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
After 10 g of (RS)-4-hydroxy-3-methyl-2-(2,2,2-trifluoroethyl)cyclopent-2-en-1-one and 4.2 g of imidazole were dissolved in 100 ml of dry dimethylformamide, 8.54 g of t-butyldimethylchlorosilane was added to the solution at an ambient temperature. After stirring at an ambient temperature for 12 hours, the reaction solution was added to 5% aqueous citric acid under ice-water cooling, and extracted three times with diethyl ether. The combined organic layer was washed successively with a saturated sodium hydrogencarbonate solution and a saturated sodium chloride solution, and dried with anhydrous magnesium sulfate. After removal of the solvent under reduced pressure, the residue was subjected to silica gel column chromatography to yield 14.3 g of (RS)-4-t-butyldimethylsilyloxy-3-methyl-2-(2,2,2-trifluoroethyl)cyclopent-2-en-1-one. Yield 90% (Eluent: n-hexane/ethyl acetate=5/1 (v/v))
후처리
- extractionextracted three times with diethyl ether
- washThe combined organic layer was washed successively with a saturated sodium hydrogencarbonate solution
- dry with materiala saturated sodium chloride solution, and dried with anhydrous magnesium sulfate
- customAfter removal of the solvent under reduced pressure
출처 및 근거
- ORD 기록
- ord-96b0dc9639b64652989dbe9595cc6175
- 출처 데이터셋
- uspto-grants-1997_09
- 특허 번호
- US05672779
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