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m-Chloroperbenzoic acid → 2,2-Diphenyl-3-methyloxirane

HRID 845815
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인쇄 미리보기

반응식

HRID 845815 반응식
[C:1]1([C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:8][CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.ClC1C=CC=C(C(OO)=[O:24])C=1>ClCCl>[C:1]1([C:7]2([C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=3)[CH:8]([CH3:9])[O:24]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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참가 물질

4

반응물 2

HCID 70297m-Chloroperbenzoic acidHCID 2382071,1-Diphenyl-1-propene

생성물 1

HCID 110958912,2-Diphenyl-3-methyloxirane수율 98.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 2.00 g (10.3 mmol) 1,1-diphenylpropene and 2.09 g (10.4 mmol) 85% m-chloroperbenzoic acid in 15 ml dichloromethane was stirred in the dark at room temperature for 4 hours. The mixture was partitioned between dichloromethane and saturated K2CO3 solution and the organic layer was washed with brine and dried over Na2SO4. This was concentrated to give 2.14 g (98%) of 2,2-diphenyl-3-methyloxirane as a colorless oil.

후처리

  1. customThe mixture was partitioned between dichloromethane and saturated K2CO3 solution
  2. washthe organic layer was washed with brine
  3. dry with materialdried over Na2SO4
  4. concentrationThis was concentrated

출처 및 근거

ORD 기록
ord-971072672f6742d58149c350a6b00dab
출처 데이터셋
uspto-grants-1988_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04760086

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