Ammonium Acetate → 2-(4-Chlorophenoxy)-1-methylpropylamine

HRID 1900165

反応式

HRID 1900165 の反応式
C([O-])(=O)C.[NH4+:5].[Na].[Cl:7][C:8]1[CH:19]=[CH:18][C:11]([O:12][CH:13]([CH3:17])[C:14](=O)[CH3:15])=[CH:10][CH:9]=1>CO>[Cl:7][C:8]1[CH:19]=[CH:18][C:11]([O:12][CH:13]([CH3:17])[CH:14]([NH2:5])[CH3:15])=[CH:10][CH:9]=1

参加物

5

実験手順

82 g of ammonium acetate and 6.7 g of sodium cyanoborohydridc were added to a solution containing 21 g of 3-(4-chlorophenoxy)-2-butanone dissolved in 500 mL of methanol, and the reaction mixture was stirred for 20 hours at room temperature. The reaction mixture was then concentrated under reduced pressure, and 180 mL of concentrated hydrochloric acid and 100 mL of water were added to the residue. The whole mixture was extracted with 300 mL of diethyl ether. The obtained water layer was alkalifled using a 5% aqueous solution of sodium hydroxide, and then extracted with 500 mL of ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulphate, and then concentrated under reduced pressure. A fraction possessing a low boiling point was removed from the obtained oily products to afford 18 g (yield 86%) of the desired product. Refractive index: 1.5360.

後処理

  1. concentrationThe reaction mixture was then concentrated under reduced pressure, and 180 mL of concentrated hydrochloric acid and 100 mL of water
  2. additionwere added to the residue
  3. extractionThe whole mixture was extracted with 300 mL of diethyl ether
  4. extractionextracted with 500 mL of ethyl acetate
  5. washThe organic layer was washed with water
  6. dry with materialdried over anhydrous magnesium sulphate
  7. concentrationconcentrated under reduced pressure
  8. customwas removed from the obtained oily products

出典と根拠

ORDレコード
ord-88648b4a5d8b4b08939df9b55f31b2f8
出典データセット
uspto-grants-1996_11
特許番号
US05574064

関連ノート

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