Triethylamine → 2-(1-Hydroxycyclopropyl)ethyl methanesulfonate

HRID 1969388ノート

反応式

HRID 1969388 の反応式
[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

  1. stirringThe reaction was stirred at −10° C. for 1 hr at rt
  2. customquenched with 1 mL ice-water
  3. extractionThe resulted mixture was extracted with dichloromethane (20 mL×3)
  4. dry with materialThe combined organic phases were dried over Na2SO4
  5. 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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