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

Potassium Cyanide → 2-Amino-2-(3-bromophenyl)acetonitrile hydrochloride

HRID 1681808
ノート
印刷プレビュー

反応式

HRID 1681808 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=O.[Cl-:10].[NH4+:11].[C-:12]#[N:13].[K+]>CO.O>[ClH:10].[NH2:11][CH:5]([C:4]1[CH:7]=[CH:8][CH:9]=[C:2]([Br:1])[CH:3]=1)[C:12]#[N:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 9032Potassium CyanideHCID 25517Ammonium ChlorideHCID 765833-Bromobenzaldehyde

生成物 1

HCID 179796432-Amino-2-(3-bromophenyl)acetonitrile hydrochloride

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒2 回

実験手順

A solution of 3-bromobenzaldehyde (18.5 g, 0.1 mol) is dissolved in methanol (15 ml) and stirred at room temperature as a solution of ammonium chloride (5.35 g, 0.1 mol) in water (12.5 ml) is added in one portion. After thirty minutes a solution of potassium cyanide (6.5 g, 0.1 mol) in water (12.5 ml) is added in one portion and the reaction stirred overnight. The mixture is then refluxed one hour, allowed to cool, and the separated oil extracted into diethyl ether and treated with an ethereal solution of hydrogen chloride to give a brown solid. This is recrystallized by dissolving in methanol (100 ml), diluting with diethyl ether (450 ml), and refrigerating the solution overnight. The solid obtained is filtered, washed with ether, and dried (3.5 g).

後処理

  1. additionis added in one portion
  2. temperatureThe mixture is then refluxed one hour
  3. temperatureto cool
  4. extractionthe separated oil extracted into diethyl ether
  5. additiontreated with an ethereal solution of hydrogen chloride
  6. customto give a brown solid
  7. customThis is recrystallized
  8. dissolutionby dissolving in methanol (100 ml)
  9. additiondiluting with diethyl ether (450 ml)
  10. customthe solution overnight
  11. customThe solid obtained
  12. filtrationis filtered
  13. washwashed with ether
  14. customdried (3.5 g)

出典と根拠

ORDレコード
ord-056bc687e06c4507b0ae3be950f09506
出典データセット
uspto-grants-1992_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05175153

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