反応 #586102

ord-8875f359d9d14de7b83db0f79e1bddf3

反応方程式

CCC(C)(C)c1cccc(NC=O)c1C
N-(2-methyl-3-(1,1-dimethylpropyl)phenyl)form-amide
[K+].[OH-]
potassium hydroxide
CO
methanol
CCC(C)(C)c1cccc(N)c1C
3-(1,1-dimethypropyl)-2-methyl-phenylamine

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度at reflux temperature for 15 hours
  2. 2
    workup.ADDITIONis added
  3. 3
    抽出the reaction mixture is extracted with ethylacetate
  4. 4
    乾燥After drying of the organic phase over sodium sulfate and evaporation of the solvent in a water jet vacuum
  5. 5
    その他the product is purified by destillation (bp. ca. 70° C., 13,33 Pa)

実験手順

2,21 g (10.77 mmol) N-(2-methyl-3-(1,1-dimethylpropyl)phenyl)form-amide, 1,42 g (21.54 mmol) 85% potassium hydroxide and 9 ml methanol are heated under stirring at reflux temperature for 15 hours. After cooling 100 ml of water is added and the reaction mixture is extracted with ethylacetate. After drying of the organic phase over sodium sulfate and evaporation of the solvent in a water jet vacuum, the product is purified by destillation (bp. ca. 70° C., 13,33 Pa). This gives 1.7 g of 2-Methyl-3-(1,1-dimethylpropyl)phenylamine in the form of a colourless oil (89% of theory).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07767625B2uspto-grants-2010_08