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m-Chloroperbenzoic acid → 3-Allyl-4-methyl-4,5-epoxypentan-2-one

HRID 894159
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HRID 894159 반응식
[CH2:1]([CH:4]([C:8]([CH3:10])=[CH2:9])[C:5](=[O:7])[CH3:6])[CH:2]=[CH2:3].ClC1C=CC=C(C(OO)=[O:19])C=1>C(Cl)Cl>[CH2:1]([CH:4]([C:8]1([CH3:10])[O:19][CH2:9]1)[C:5](=[O:7])[CH3:6])[CH:2]=[CH2:3]
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 132086223-(Prop-1-en-2-yl)hex-5-en-2-one

생성물 1

HCID 132086283-Allyl-4-methyl-4,5-epoxypentan-2-one수율 23.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 3-allyl-4-methyl-pent-4-en-2-one (20.0 g) in methylene chloride (100 ml) was added dropwise a solution of m-chloroperbenzoic acid (29 g) in methylene chloride (300 ml) at 0° to 5° C. The reaction mixture was stirred at 0° to 5° C. for 3 hours and then at 20° C. overnight. The reaction solution was progressively washed with an aqueous sodium hydrogen carbonate solution, aqueous sodium sulfite solution, aqueous sodium hydrogen carbonate solution and then with an aqueous sodium chloride solution. After removing the solvent by evaporation, the residue was distilled to obtain 7.2 g of the unreacted material and 5.2 g of the objective 3-allyl-4-methyl-4,5-epoxy-pentan-2-one.

후처리

  1. customat 20° C.
  2. customovernight
  3. washThe reaction solution was progressively washed with an aqueous sodium hydrogen carbonate solution, aqueous sodium sulfite solution, aqueous sodium hydrogen carbonate solution
  4. customAfter removing the solvent
  5. customby evaporation
  6. distillationthe residue was distilled

출처 및 근거

ORD 기록
ord-79939989016f4a7e8e36cb4cfdc8070f
출처 데이터셋
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04282372

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