반응식
[C:1]([O:6][CH3:7])(=O)[C@@H:2](C)O.[H-].[Na+].[C:10]([O:14][CH3:15])(=[O:13])[CH:11]=[CH2:12].S(=O)(=O)(O)[OH:17]>C(OCC)C.CS(C)=O>[CH3:15][O:14][C:10]([CH:11]1[CH2:7][O:6][C@H:1]([CH3:2])[C:12]1=[O:17])=[O:13]참가 물질
반응 조건
- 온도
- -35 °C
실험 절차
A solution of methyl (R)-(+)-lactate (30 g) in diethyl ether (60 ml) was added dropwise to a stirred mixture of sodium hydride (65%, 10.42 g) and diethyl ether (180 ml) which had been cooled to -35° C. The mixture was allowed to warm to 0° C. and stirred for 20 minutes. The mixture was evaporated. To the residue so obtained there was added a solution of methyl acrylate (29.2 ml) in DMSO (120 ml) which had been cooled to 10° C. The mixture was stirred in an ice-bath for 30 minutes and at ambient temperature for 2 hours. The mixture was poured into cold dilute (5%) aqueous sulphuric acid and extracted with diethyl ether. The organic phase was washed with a cold aqueous sodium bicarbonate solution and with brine, dried (MgSO4) and evaporated. The residue was distilled to give (2R)-4-methoxycarbonyl-2-methyltetrahydrofuran-3-one (16.5 g, 37%), b.p. 66°-68° C. (0.5 mm Hg), [alpha]20 =+55.3° (conc.=1.16 g per 100 ml of chloroform).
후처리
- temperatureto warm to 0° C.
- customThe mixture was evaporated
- customTo the residue so obtained there
- temperaturehad been cooled to 10° C
- stirringThe mixture was stirred in an ice-bath for 30 minutes and at ambient temperature for 2 hours
- additionThe mixture was poured
- extractionextracted with diethyl ether
- washThe organic phase was washed with a cold aqueous sodium bicarbonate solution and with brine
- dry with materialdried (MgSO4)
- customevaporated
- distillationThe residue was distilled
출처 및 근거
- ORD 기록
- ord-4dfdbc038b83474dbb86e11ebae6e988
- 출처 데이터셋
- uspto-grants-1996_01
- 특허 번호
- US05482966
연결된 노트
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