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

Ethanolamine → HCID 54468234、化合物

HRID 864281
ノート
印刷プレビュー

反応式

HRID 864281 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[CH:9][CH2:10][O:11][N:12]2C(=O)C3=CC=CC=C3C2=O)=[CH:4][CH:3]=1.C(CN)O>ClCCl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[CH:9][CH2:10][O:11][NH2:12])=[CH:6][CH:7]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 700EthanolamineHCID 54486942HCID 54486942、化合物

生成物 1

HCID 54468234HCID 54468234、化合物収率 95.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
30 °C

実験手順

33.4 g (0.093 mol) of N-[3-(4-bromophenyl)-prop-2-enyloxy]-phthalimide were introduced a little at a time into 50 ml of ethanolamine; the temperature increased to 30° C. After stirring had been carried out for two hours at 60° C., the mixture was allowed to cool and 200 ml of dichloromethane were added to it. It was extracted by shaking with iced water. The organic phase was dried and evaporated down and the residue was crystallized from petroleum ether. 20.2 g (95.3% of theory) of 3-(4-bromophenyl)-prop-2-enyloxyamine of melting point 35°-38° C. were obtained.

後処理

  1. temperatureto cool
  2. extractionIt was extracted
  3. stirringby shaking with iced water
  4. customThe organic phase was dried
  5. customevaporated down
  6. customthe residue was crystallized from petroleum ether

出典と根拠

ORDレコード
ord-e95b325da54f4240808b57cbe4101d8b
出典データセット
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05563114

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート