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Ammonia → HCID 10081732、化合物

HRID 1732245
ノート
印刷プレビュー

反応式

HRID 1732245 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 2 M 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.

後処理

  1. filtration
The reaction mixture was filtered
  • concentrationthe filtrate concentration in vacuo
  • dissolutionThe residue was dissolved in 2 M hydrochloric acid
  • extractionwas extracted with ethyl acetate
  • extractionwas extracted with methylene chloride
  • 出典と根拠

    ORDレコード
    ord-0d23a45efa82471b8acc1ae6dcda1c9c
    出典データセット
    uspto-grants-1980_12
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04237068

    反応ノート

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    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