Acetone → 2-Propenylphenyloxymethyl methyl ketone

HRID 43284

반응식

HRID 43284 반응식
[CH:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])=[CH:2][CH3:3].C(=O)([O-])[O-].[K+].[K+].[CH3:17][C:18]([CH3:20])=[O:19].ClCC(=O)C>[I-].[K+].O>[CH3:17][C:18]([CH2:20][O:10][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[CH:1]=[CH:2][CH3:3])=[O:19]

참가 물질

7

실험 절차

A mixture of 7.112 g (50.0 mmol) of 2-propenylphenol (E/Z mixture), 7.041 g of potassium carbonate (50.0 mmol) and 20 ml of acetone was stirred at the boiling point under reflux for 20 minutes. A mixture of 6.94 g (75.0 mmol) of chloroacetone, 0.171 g (1.0 mmol) of potassium iodide and 6.5 ml of acetone which had been activated beforehand by stirring overnight at room temperature was then added to the reaction mixture and the reaction mixture was stirred overnight at the boiling point under reflux. The reaction mixture was cooled to room temperature, added to 50 ml of water and extracted three times with 40 ml each time of diethyl ether. The organic phase was washed with 5% strength sodium hydroxide solution, separated off, dried over Na2SO4 and evaporated. Distillation of the crude product under reduced pressure gave 6.788 g (yield: 67% of theory) of 2-propenylphenyloxymethyl methyl ketone of the formula 2a:

후처리

  1. temperatureunder reflux for 20 minutes
  2. stirringby stirring overnight at room temperature
  3. additionwas then added to the reaction mixture
  4. stirringthe reaction mixture was stirred overnight at the boiling point
  5. temperatureunder reflux
  6. extractionextracted three times with 40 ml each time of diethyl ether
  7. washThe organic phase was washed with 5% strength sodium hydroxide solution
  8. customseparated off
  9. dry with materialdried over Na2SO4
  10. customevaporated
  11. distillationDistillation of the crude product under reduced pressure

출처 및 근거

ORD 기록
ord-c1169901726341f8961822700365ee8b
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08536344B2

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