反応式
[CH3:1][S:2]([O:5]S(C)(=O)=O)(=[O:4])=[O:3].[CH3:10][C@@H:11](O)[CH2:12][CH3:13].C(N(CC)CC)C>ClCCl>[CH3:1][S:2]([O:5][C@H:11]([CH3:10])[CH2:12][CH3:13])(=[O:4])=[O:3]参加物
5
実験手順
A solution of methanesulphonic anhydride (8.33 g, 47.8 mmol) in dichloromethane (30 ml) was added dropwise over 30 minutes to an ice-cooled solution of (R)-2-butanol (4.0ml, 43.5 mmol) and triethylamine (6.65 ml, 47.8 mmol) in dichloromethane (70 ml). The reaction was then allowed to warm to room temperature and stirred for 18 hours. The mixture was then washed with water, 2N hydrochloric acid, then dried (Na2SO4) and evaporated under reduced pressure to give the title compound as a pale yellow oil, 7.0 g.
後処理
- washThe mixture was then washed with water, 2N hydrochloric acid
- dry with materialdried (Na2SO4)
- customevaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-c666a9cb353045a88b0d68fbaf799a5a
- 出典データセット
- uspto-grants-2004_01
- 特許番号
- US06677335B1
関連ノート
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