乙酸铵 → 1-(4-Chloro-2-methylphenoxy)propan-2-amine

HRID 924

反应方程式

HRID 924 反应方程式
C([O-])(=O)C.[NH4+].C([BH3-])#[N:7].[Na+].[Cl:10][C:11]1[CH:21]=[CH:20][C:14]([O:15][CH2:16][C:17](=O)[CH3:18])=[C:13]([CH3:22])[CH:12]=1>CO>[Cl:10][C:11]1[CH:21]=[CH:20][C:14]([O:15][CH2:16][CH:17]([NH2:7])[CH3:18])=[C:13]([CH3:22])[CH:12]=1

参与物

5

实验过程

120 g of ammonium acetate and 9.8 g of sodium cyanoborohydride were added to a solution containing 31 g of (4-chloro-2-methylphenoxy)acetone dissolved in 700 mL of methanol, and the resultant mixture was stirred for 20 hours at room temperature. After the reaction mixture was concentrated under reduced pressure. 180 mL of concentrated hydrochloric acid and 100 mL of water were added to the residue. The whole mixture was stirred for 1 hour, and then extracted with 300 mL of diethyl ether. The water layer was alkalified 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 sulfate, and then concentrated under reduced pressure. A fraction possessing a low boiling point was removed from the obtained oily products to afford 25 g (yield 81%) of the desired product. Refractive index: 1.5360.

后处理

  1. concentrationAfter the reaction mixture was concentrated under reduced pressure
  2. addition180 mL of concentrated hydrochloric acid and 100 mL of water were added to the residue
  3. extractionextracted 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 sulfate
  7. concentrationconcentrated under reduced pressure
  8. customwas removed from the obtained oily products

来源与证据

ORD记录
ord-765c60307caa49c8b39c2317a5db5d9f
来源数据集
uspto-grants-1998_03
专利号
US05723469

关联笔记

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