Sulfuric Acid → Methyl 3-amino-2,4,6-trimethylphenylacetate

HRID 2229903ノート

反応式

HRID 2229903 の反応式
[C:1]([CH2:3][C:4]1[C:5]([CH3:13])=[C:6]([C:8]([CH3:12])=[CH:9][C:10]=1[CH3:11])[NH2:7])#N.S(=O)(=O)(O)[OH:15].[C:19](=O)([O-])[O-:20].[Na+].[Na+]>CO.O>[NH2:7][C:6]1[C:5]([CH3:13])=[C:4]([CH2:3][C:1]([O:20][CH3:19])=[O:15])[C:10]([CH3:11])=[CH:9][C:8]=1[CH3:12]

参加物

6

反応物 3

HCID 1118Sulfuric AcidHCID 10340Sodium CarbonateHCID 108449753-Cyanomethyl-2,4,6-trimethylaniline

生成物 1

HCID 10560264Methyl 3-amino-2,4,6-trimethylphenylacetate収率 88%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒2 回HCID 962Water溶媒

実験手順

To a solution of 3-cyanomethyl-2,4,6-trimethylaniline (see Example 14, procedure C) (5 g, 28.7 mmol) in methanol (30 mL) was added concentrated sulfuric acid (30 mL) with cooling. The resulting mixture was heated under reflux for 8 h before it was allowed to cool to rt and diluted with water (100 mL). The mixture was stripped off methanol and the residue was basified with sodium carbonate and then extracted with ethyl acetate. The organic layer was worked up and concentrated as usual to give the desired compound as an oil (5.2 g, 88%).

後処理

  1. temperaturewith cooling
  2. temperatureThe resulting mixture was heated
  3. temperatureunder reflux for 8 h before it
  4. extractionextracted with ethyl acetate
  5. concentrationconcentrated as usual

出典と根拠

ORDレコード
ord-b47951e02e7e46fc8bafa2f30a51b8a4
出典データセット
uspto-grants-2002_07
特許番号
US06420567B1

反応ノート

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