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Benzoyl Peroxide → HCID 14368704, 화합물

HRID 1195834
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HRID 1195834 반응식
[F:1][C:2]1[CH:11]=[C:10]([F:12])[CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[CH3:13].[Br:14]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[F:1][C:2]1[CH:11]=[C:10]([F:12])[CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[CH2:13][Br:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 14368703HCID 14368703, 화합물

생성물 1

HCID 14368704HCID 14368704, 화합물

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

1.35 g of 5,7-Difluoro-1-methylnaphthaline in 10 ml of carbon tetrachloride are refluxed for 41/2 hours with 1.4 g of N-bromosuccinimide and 50 mg of dibenzoylperoxide. The cooled mixture is filtered and the solvent removed under vacuum. The purity of the crystalline crude product is sufficient for further reaction, m.p. 74°-76.5°.

후처리

  1. filtrationThe cooled mixture is filtered
  2. customthe solvent removed under vacuum
  3. customThe purity of the crystalline crude product is sufficient for further reaction, m.p. 74°-76.5°

출처 및 근거

ORD 기록
ord-8c79336066a24a918e8010e041886d60
출처 데이터셋
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05112851

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