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

3-Chloro-2-methylaniline → N-(3-Chloro-2-methylphenyl)-3-nitropyridin-2-amine

HRID 614333
ノート
印刷プレビュー

反応式

HRID 614333 の反応式
Cl[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[Cl:11][C:12]1[C:13]([CH3:19])=[C:14]([CH:16]=[CH:17][CH:18]=1)[NH2:15]>>[Cl:11][C:12]1[C:13]([CH3:19])=[C:14]([CH:16]=[CH:17][CH:18]=1)[NH:15][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=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

3

反応物 2

HCID 68943-Chloro-2-methylanilineHCID 796132-Chloro-3-nitropyridine

生成物 1

HCID 12445357N-(3-Chloro-2-methylphenyl)-3-nitropyridin-2-amine

反応条件

温度
50 °C

実験手順

A mixture of 6.3 g. (0.04 mole) of 2-chloro-3-nitropyridine and 16.9 g. (0.12 mole) of 3-chloro-2-methylaniline was heated in an oil bath to 170° C. when the temperature spontaneously rose to 185° C. After an additional 10 minutes at 180° C., the mixture was cooled to 50° C. and extracted with a solution of 75 ml. of water and 25 ml. of acetic acid. The insolubles were collected, air dried, dissolved in methylene chloride, and the solution was dried over magnesium sulfate. The solution was concentrated to a small volume and diluted with 50 ml. of ether which caused crystallization of 6.6 g. of 2-(3-chloro-2-methylanilino)-3-nitropyridine, m.p. 134°-135° C.

後処理

  1. additionA mixture of 6.3 g
  2. customspontaneously rose to 185° C
  3. extractionextracted with a solution of 75 ml
  4. customThe insolubles were collected
  5. customair dried
  6. dissolutiondissolved in methylene chloride
  7. dry with materialthe solution was dried over magnesium sulfate
  8. concentrationThe solution was concentrated to a small volume
  9. additiondiluted with 50 ml
  10. customcrystallization of 6.6 g

出典と根拠

ORDレコード
ord-e2712bac3eaf4fe58e6e3246ef394e06
出典データセット
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04144341

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