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Benzoyl Peroxide → 5-(3-Bromomethylphenyl)isoxazole

HRID 2254407
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반응식

HRID 2254407 반응식
[CH3:1][C:2]1[CH:3]=[C:4]([C:8]2[O:12][N:11]=[CH:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1.[Br:13]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[Br:13][CH2:1][C:2]1[CH:3]=[C:4]([C:8]2[O:12][N:11]=[CH:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 197446775-(m-Tolyl)isoxazole

생성물 1

HCID 197446715-(3-Bromomethylphenyl)isoxazole

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

106 mg of 5-(3-methylphenyl)isoxazole, 119 mg of N-bromosuccinimide and 2 mg of benzoyl peroxide were dissolved in 10 ml of carbon tetrachloride, and the solution was refluxed for 3 hours with stirring. After cooling, the precipitate was separated by filtration, and concentrated under reduced pressure to give 5-(3-bromomethylphenyl)isoxazole as a pale yellow oily product.

후처리

  1. temperaturethe solution was refluxed for 3 hours
  2. temperatureAfter cooling
  3. customthe precipitate was separated by filtration
  4. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-3b6a53edcdec44a5aea4950aa6624dc7
출처 데이터셋
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05234946

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