Triethylamine → 2-(1-Hydroxycyclopropyl)ethyl methanesulfonate
反応式
[OH:1][CH2:2][CH2:3][C:4]1([OH:7])[CH2:6][CH2:5]1.C(N(CC)CC)C.[CH3:15][S:16](Cl)(=[O:18])=[O:17]>ClCCl>[CH3:15][S:16]([O:1][CH2:2][CH2:3][C:4]1([OH:7])[CH2:6][CH2:5]1)(=[O:18])=[O:17]参加物
5
反応条件
- 温度
- -10 °C
実験手順
A mixture of 1-(2-hydroxyethyl)cyclopropanol (86 mg, 0.843 mmol) and triethylamine (136 mg, 1.35 mmol, Shantou Xilong chemical factory) in 10 mL of dichloromethane was stirred at −10° C. for 30 min. Methanesulfonyl chloride (106 mg, 0.927 mmol, Shanghai Haiqu chemical Ltd.) was then added via a syringe. The reaction was stirred at −10° C. for 1 hr at rt and then quenched with 1 mL ice-water. The resulted mixture was extracted with dichloromethane (20 mL×3). The combined organic phases were dried over Na2SO4 and concentrated in vacuo to afford 2-(1-hydroxycyclopropyl)ethyl methanesulfonate as yellow oil (used in the next step without further purification).
後処理
- stirringThe reaction was stirred at −10° C. for 1 hr at rt
- customquenched with 1 mL ice-water
- extractionThe resulted mixture was extracted with dichloromethane (20 mL×3)
- dry with materialThe combined organic phases were dried over Na2SO4
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-983862b061ee443fbf3987d51b76e7f3
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08426585B2
反応ノート
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