ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Triethylamine → 2-(Benzylsulfanyl)ethyl 2-bromopropanoate

HRID 65390
ノート
印刷プレビュー

反応式

HRID 65390 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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 774862-(Benzylthio)ethanolHCID 79047Propanoyl bromide, 2-bromo-

生成物 1

HCID 133096302-(Benzylsulfanyl)ethyl 2-bromopropanoate

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒2 回

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.

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-ab37ea9144714543bff7be74a09a002f
出典データセット
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04614536

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート