反応式
[CH:1]1([CH2:4][CH2:5][OH:6])[CH2:3][CH2:2]1.C(N(CC)CC)C.[CH3:14][S:15](Cl)(=[O:17])=[O:16].O>C(OCC)(=O)C>[CH3:14][S:15]([O:6][CH2:5][CH2:4][CH:1]1[CH2:3][CH2:2]1)(=[O:17])=[O:16]参加物
6
実験手順
A 0.5 g quantity of 2-cyclopropylethanol and 3.1 ml of triethylamine were dissolved in 10 ml of ethyl acetate, and 0.75 ml of methanesulfonyl chloride was added with ice-cooling and stirring. After stirring for 30 minutes, water was added to the reaction mixture and extraction was performed. The organic layer was washed with water twice and concentrated by removing the solvent under reduced pressure to give 1 g of pale yellow oily 2-cyclopropylethyl methanesulfonate.
後処理
- temperaturecooling
- stirringAfter stirring for 30 minutes
- washThe organic layer was washed with water twice
- concentrationconcentrated
- customby removing the solvent under reduced pressure
出典と根拠
- ORDレコード
- ord-9027ce4a434f4a6d8f1ff10f40755bef
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08637559B2
関連ノート
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