反応式
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]参加物
5
反応条件
- 温度
- 108.5 °C
実験手順
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.).
後処理
- temperaturecooled to about 28° C. (inner temperature)
- additionwere added
- extractionthe mixture was extracted
- washThe organic layer was washed twice with water (400 mL)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-73ccc542e7174b7aa2f0aab166d67b5b
- 出典データセット
- uspto-grants-2012_09
- 特許番号
- US08273916B2
関連ノート
読み込み中…