Phenylacetic Acid → N-butyl-2-phenylacetamide

HRID 70077ノート

反応式

HRID 70077 の反応式
[C:1]1([CH2:7][C:8]([OH:10])=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:11]([NH2:15])[CH2:12][CH2:13][CH3:14]>S(=O)(=O)(O)O.CO>[CH2:11]([NH:15][C:8](=[O:10])[CH2:7][C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[CH2:12][CH2:13][CH3:14]

参加物

5

反応物 2

HCID 999Phenylacetic AcidHCID 8007Butylamine

生成物 1

HCID 221447N-butyl-2-phenylacetamide収率 70.7%

試薬・触媒・溶媒 2

HCID 1118Sulfuric Acid触媒HCID 887Methanol溶媒

実験手順

Phenylacetic acid (16 g, 117.6 mmol) and methanol (60 ml) were added to a 250 ml three-necked flask, followed by addition of 5 drops of concentrated sulphuric acid. The resulting solution was heated to reflux for 6 hours. Then, the mixture was cooled to room temperature, followed by adding n-butylamine (12 ml, 121.4 mmol), and heated to reflux for another 3 hours. After the reaction was completed, it was cooled to room temperature. Most of the solvent was removed by rotary vacuum evaporation, 30 ml of water was added thereinto, and the mixture was extracted with ethyl acetate (3×80 ml). The combined organic layer was dried over anhydrous magnesium sulfate, filtrated, and concentrated under reduced pressure to yield 15.9 g of N-n-butylphenylacetamide (white solid, yield: 70.4%).

後処理

  1. temperatureThe resulting solution was heated
  2. temperatureto reflux for 6 hours
  3. temperatureheated
  4. temperatureto reflux for another 3 hours
  5. temperatureit was cooled to room temperature
  6. customMost of the solvent was removed by rotary vacuum evaporation, 30 ml of water
  7. additionwas added
  8. extractionthe mixture was extracted with ethyl acetate (3×80 ml)
  9. dry with materialThe combined organic layer was dried over anhydrous magnesium sulfate
  10. filtrationfiltrated
  11. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-1a2e6e511c55421aa16f0a2d192fcf97
出典データセット
uspto-grants-2014_09
特許番号
US08822519B2

反応ノート

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