反応式
[CH:1]1([CH2:4][CH2:5][OH:6])[CH2:3][CH2:2]1.ClCCl.[CH3:10][S:11](Cl)(=[O:13])=[O:12].C(N(CC)CC)C>C(OCC)(=O)C.O>[CH3:10][S:11]([O:6][CH2:5][CH2:4][CH:1]1[CH2:3][CH2:2]1)(=[O:13])=[O:12]参加物
7
実験手順
To a mixture of 2-cyclopropylethanol (5.35 g, 62.1 mmol) and dichloromethane (107 mL) were added methanesulfonyl chloride (5.29 mL, 68.3 mmol) and triethylamine (13.1 mL, 93.1 mmol) in that order while stirring on ice, and the resulting mixture was stirred for 1 hour. Water and ethyl acetate were then added to the reaction mixture. After thoroughly shaking the mixture, the organic layer was separated and the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The mixture was then filtered, and the solvent in the filtrate was distilled off under reduced pressure to obtain the title compound (10.3 g, 62.7 mmol).
後処理
- stirringthe resulting mixture was stirred for 1 hour
- stirringAfter thoroughly shaking the mixture
- customthe organic layer was separated
- washthe organic layer was washed with brine
- dry with materialdried over anhydrous magnesium sulfate
- filtrationThe mixture was then filtered
- distillationthe solvent in the filtrate was distilled off under reduced pressure
出典と根拠
- ORDレコード
- ord-8cc13b95ca8b4518a5dbae1952f6e897
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08530504B2
関連ノート
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