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Benzoyl Peroxide → 3-Bromomethyl-5-chloro-2-phenylbenzo[b]thiophene

HRID 1246394
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HRID 1246394 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[C:7]([CH3:16])[C:6]=2[CH:17]=1.[Br:18]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C(Cl)(Cl)(Cl)Cl>[Br:18][CH2:16][C:7]1[C:6]2[CH:17]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=2[S:9][C:8]=1[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7187Benzoyl PeroxideHCID 67184N-bromobutanimideHCID 8219825-Chloro-3-methyl-2-phenyl-1-benzothiophene

생성물 1

HCID 219167743-Bromomethyl-5-chloro-2-phenylbenzo[b]thiophene

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

In a 100 ml round-bottomed flask, 1 eq. of the compound obtained in Step B is dissolved in 20 ml of CCl4. 1 eq. of N-bromosuccinimide and 0.04 eq. of benzoyl peroxide are then added, and the mixture is irradiated by means of a halogen lamp and maintained at reflux for 4 hours. At the end of the reaction, the insoluble material is filtered off, and the carbon tetrachloride is evaporated off. The residue obtained is purified by chromatography on a silica gel column.

후처리

  1. customthe mixture is irradiated by means of a halogen lamp
  2. temperaturemaintained
  3. temperatureat reflux for 4 hours
  4. customAt the end of the reaction
  5. filtrationthe insoluble material is filtered off
  6. customthe carbon tetrachloride is evaporated off
  7. customThe residue obtained
  8. customis purified by chromatography on a silica gel column

출처 및 근거

ORD 기록
ord-b634f72e6ec846d3ba2e8fc91d284af3
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07126012B2

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