Sodium hydride → 3-(3,3-Diethoxypropoxy)-2-methylprop-1-ene
반응식
[CH2:1]([O:3][CH:4]([O:8][CH2:9][CH3:10])[CH2:5][CH2:6][OH:7])[CH3:2].[H-].[Na+].Br[CH2:14][C:15]([CH3:17])=[CH2:16]>C1COCC1>[CH2:1]([O:3][CH:4]([O:8][CH2:9][CH3:10])[CH2:5][CH2:6][O:7][CH2:16][C:15]([CH3:17])=[CH2:14])[CH3:2]참가 물질
5
실험 절차
To a stirred solution of 3,3-diethoxy-1-propanol (3.0 g, 22.2 mmol) in anhydrous THF (50 mL) was added sodium hydride (60% dispersion in mineral oil, 1.07 g, 26.6 mmol). The reaction mixture was stirred for 30 minutes, and 3-bromo-2-methyl-1-propene (3.63 g, 24.5 mmol) then added. The reaction mixture was then stirred for a further 18 hours. The reaction mixture was quenched with saturated sodium hydrogen carbonate and extracted with ethyl acetate (×3). The combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution and brine, dried (sodium sulfate), filtered and concentrated under reduced pressure to afford an oil (2.25 g, 50%). The material used in the next step without further purification.
후처리
- stirringThe reaction mixture was then stirred for a further 18 hours
- customThe reaction mixture was quenched with saturated sodium hydrogen carbonate
- extractionextracted with ethyl acetate (×3)
- washThe combined organic extracts were washed with saturated aqueous sodium hydrogen carbonate solution and brine
- dry with materialdried (sodium sulfate)
- filtrationfiltered
- concentrationconcentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-f6fd28a8e9c648ed9a08fe5b3921417c
- 출처 데이터셋
- uspto-grants-2015_04
- 특허 번호
- US09012644B2
반응 노트
불러오는 중…