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

Ammonia → HCID 10081732、化合物

HRID 1856298
ノート
印刷プレビュー

反応式

HRID 1856298 の反応式
Br[CH:2]([CH3:15])[C:3]([NH:5][C:6]1[C:11]([CH3:12])=[CH:10][CH:9]=[CH:8][C:7]=1[CH2:13][CH3:14])=[O:4].[NH3:16]>>[NH2:16][CH:2]([CH3:15])[C:3]([NH:5][C:6]1[C:11]([CH3:12])=[CH:10][CH:9]=[CH:8][C:7]=1[CH2:13][CH3:14])=[O:4]
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 222Ammonia2 回HCID 4392336Propanamide, 2-bromo-N-(2-ethyl-6-methylphenyl)-

生成物 1

HCID 10081732HCID 10081732、化合物

反応条件

温度
55 °C

実験手順

A slurry of 20.9 g 2-bromo-2'-ethyl-6'-methyl propionanilide, 125 ml 95% alcohol, and 75 ml concd. ammonia was saturated with gaseous ammonia and was heated to 55° C. for 30 hours in a pressure vessel. The reaction mixture was filtered and the filtrate concentration in vacuo. The residue was dissolved in 2M hydrochloric acid and was extracted with ethyl acetate. The acid phase was made alkaline to pH 9 and was extracted with methylene chloride to give 15.5 g of a crystallizing oil. Recrystallized from ether-petroleum ether, the compound (2-amino-2'-ethyl-6'-methylpropionanilide) melted at 68.5°-70° C. Calcd. for C12H18N2O: C 69.8, H 8.79, N 13.6. Found: C 69.7, N 8.72, N 13.5.

後処理

  1. filtrationThe reaction mixture was filtered
  2. concentrationthe filtrate concentration in vacuo
  3. dissolutionThe residue was dissolved in 2M hydrochloric acid
  4. extractionwas extracted with ethyl acetate
  5. extractionwas extracted with methylene chloride

出典と根拠

ORDレコード
ord-fdc84165a83b412a8268fe94de344e64
出典データセット
uspto-grants-1980_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04218477

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