Réaction #586102

ord-8875f359d9d14de7b83db0f79e1bddf3

Équation de réaction

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

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07767625B2uspto-grants-2010_08