반응식
C([Li])CCC.[CH3:6][CH:7]1[S:12][CH2:11][CH2:10][CH2:9][S:8]1.[CH:13](=[O:17])[CH2:14][CH2:15][CH3:16].O>CCCCCC.O1CCCC1>[OH:17][CH:13]([C:7]1([CH3:6])[S:12][CH2:11][CH2:10][CH2:9][S:8]1)[CH2:14][CH2:15][CH3:16]참가 물질
반응 조건
- 온도
- -30 °C
실험 절차
56 mmol of n-butyllithium (35 ml of a 1.6 M solution in hexane) were added with stirring to a solution of 2-methyl-1,3-dithian (7 g, 52.1 mmol) in 100 ml of dry tetrahydrofuran at −30° C. under argon. After stirring at −30° C. for 2 hours, the mixture was cooled to −78° C. 4.2 g (58.3 mmol) of freshly distilled n-butyraldehyde were added dropwise in the course of 15 minutes and the mixture was stirred for a further 30 minutes. After warming to 20° C., it was poured into a beaker containing 300 ml of water and 100 ml of n-hexane. The organic phase was separated off and the aqueous phase was extracted three times with 50 ml of dichloromethane in each case. The combined organic phases were washed with 10% strength by weight potassium hydroxide solution, water and concentrated sodium chloride solution, dried over anhydrous sodium sulfate and then distilled. 8.82 g of 2-(1-hydroxybutyl)-2-methyl-1,3-dithian were isolated as a colorless oil.
후처리
- temperaturethe mixture was cooled to −78° C
- stirringthe mixture was stirred for a further 30 minutes
- temperatureAfter warming to 20° C.
- additionit was poured into a beaker
- customThe organic phase was separated off
- extractionthe aqueous phase was extracted three times with 50 ml of dichloromethane in each case
- washThe combined organic phases were washed with 10% strength by weight potassium hydroxide solution, water and concentrated sodium chloride solution
- dry with materialdried over anhydrous sodium sulfate
- distillationdistilled
출처 및 근거
- ORD 기록
- ord-4a3edc1b5e0642e8be21e20e3154a1ca
- 출처 데이터셋
- uspto-grants-2001_06
- 특허 번호
- US06245328B1
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