Triethylamine → 2-(Benzylsulfanyl)ethyl 2-bromopropanoate

HRID 615542

反応式

HRID 615542 の反応式
[Br:1][CH:2]([CH3:6])[C:3](Br)=[O:4].C(N(CC)CC)C.[CH2:14]([S:21][CH2:22][CH2:23][OH:24])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C1(C)C=CC=CC=1>[Br:1][CH:2]([CH3:6])[C:3]([O:24][CH2:23][CH2:22][S:21][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:4]

参加物

5

実験手順

A solution of 21.6 g of 2-bromopropionyl bromide in 30 ml of toluene was added dropwise to a solution of 10.1 g of triethylamine and 16.8 g of 2-benzylthioethanol in 150 ml of toluene at room temperature whilst stirring. After the addition was completed, the reaction mixture was stirred for a further 2 hours at room temperature. The mixture was then washed successively with 1% strength by weight aqueous solution of sodium hydroxide and water. After drying the organic phase over anhydrous sodium sulphate, the toluene was distilled off under reduced pressure, and the end product of 2-benzylthioethyl 2-bromopropionate was obtained in a yield of 28.8 g as a colorless product. nD20 =1.5570.

後処理

  1. additionAfter the addition
  2. stirringthe reaction mixture was stirred for a further 2 hours at room temperature
  3. washThe mixture was then washed successively with 1% strength by weight aqueous solution of sodium hydroxide and water
  4. dry with materialAfter drying the organic phase over anhydrous sodium sulphate
  5. distillationthe toluene was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-b88167dfb4ec4c39ad1b33673fca9657
出典データセット
uspto-grants-1985_02
特許番号
US04500346

関連ノート

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