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

Chloroform → alpha-Chloro-3-nitrobenzaldoxime

HRID 917984
ノート
印刷プレビュー

反応式

HRID 917984 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][CH:12]=1)[CH:7]=[N:8][OH:9])([O-:3])=[O:2].C(Cl)(Cl)[Cl:14]>>[Cl:14][C:7](=[N:8][OH:9])[C:6]1[CH:10]=[CH:11][CH:12]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 6212ChloroformHCID 2191323-Nitrobenzaldoxime

生成物 1

HCID 2756318alpha-Chloro-3-nitrobenzaldoxime収率 93.7%

実験手順

32.9 g (0.2 mol) of 3-nitrobenzaldoxime was suspended in 150 g of chloroform and chlorine gas was bubbled into the suspension while maintaining the reaction mixture at a temperature of from 5° to 10°C. 3-Nitrobenzaldoxime went into solution showing a green color upon reaction with chlorine to give a reaction mixture having a deep green color. The reaction mixture turned a pale yellowish-brown upon standing; chloroform was then removed from the reaction mixture under reduced pressure to give 37.6 g of pale yellow crystals having a melting point of 98°-101°C. Yield, 94%.

後処理

  1. customchlorine gas was bubbled into the suspension
  2. temperaturewhile maintaining the reaction mixture at a temperature of from 5° to 10°C
  3. customupon reaction with chlorine
  4. customto give a reaction mixture
  5. customchloroform was then removed from the reaction mixture under reduced pressure

出典と根拠

ORDレコード
ord-cfd7774f68ec48e99a7b05785d481d4f
出典データセット
uspto-grants-1976_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03968240

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