반응식
CS(O)(=O)=O.[CH3:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].C(O[CH:17]([CH3:19])[CH3:18])(=O)C.[C:20]([OH:23])(=[O:22])C>O>[CH2:8]([C@H:9]([CH2:10][CH2:11][CH2:12][CH2:18][CH2:17][CH3:19])[C:20]([OH:23])=[O:22])[CH2:7][CH3:6]참가 물질
5
반응 조건
- 온도
- 108.5 °C
실험 절차
Under an argon atmosphere, the compound (100 g) produced in Reference Example 3 was dissolved in acetic acid (230 mL) at about 40° C. (inner temperature). A solution of methanesulfonic acid (130 g) in water (182 mL) was added to the above solution, then stirred at about 105-112° C. (inner temperature) for about 13 hours, and cooled to about 28° C. (inner temperature). Then, water (400 mL) and a mixture of n-heptane: isopropyl acetate (5:1) (500 mL) were added and the mixture was extracted. The organic layer was washed twice with water (400 mL) and concentrated to give (2R)-2-propyloctanoic acid having the following physicochemical properties (103 g, 99.3% e.e.).
후처리
- temperaturecooled to about 28° C. (inner temperature)
- additionwere added
- extractionthe mixture was extracted
- washThe organic layer was washed twice with water (400 mL)
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-73ccc542e7174b7aa2f0aab166d67b5b
- 출처 데이터셋
- uspto-grants-2012_09
- 특허 번호
- US08273916B2
연결된 노트
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