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N-bromobutanimide → 3-Bromomethyl-4-chloro-5-methyl-benzonitrile

HRID 2194790
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HRID 2194790 반응식
[Cl:1][C:2]1[C:9]([CH3:10])=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[CH3:11].[Br:12]N1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>[Br:12][CH2:10][C:9]1[CH:8]=[C:5]([CH:4]=[C:3]([CH3:11])[C:2]=1[Cl:1])[C:6]#[N:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 67184N-bromobutanimideHCID 575173244-Chloro-3,5-dimethyl-benzonitrile

생성물 1

HCID 670504963-Bromomethyl-4-chloro-5-methyl-benzonitrile수율 66.6%

시약·촉매·용매 2

HCID 7187Benzoyl Peroxide촉매HCID 5943Carbon Tetrachloride용매

실험 절차

A mixture of 4-chloro-3,5-dimethyl-benzonitrile (1.011 g, 6.10 mmol), N-bromosuccinimide (1.087 g, 6.10 mmol) and benzoyl peroxide (0.074 g, 0.305 mmol) in carbon tetrachloride (30 mL) was heated to reflux for 4 hr. The reaction mixture was cooled to room temperature and filtered. The filtrate was purified by flash column chromatography (silica gel, 0 to 30% ethyl acetate/hexane) to give 3-bromomethyl-4-chloro-5-methyl-benzonitrile as an impure white solid (0.9938 g, 66%), which was used in the next step without further purification.

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후처리

  1. temperaturewas heated
  2. temperatureto reflux for 4 hr
  3. filtrationfiltered
  4. customThe filtrate was purified by flash column chromatography (silica gel, 0 to 30% ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-4042390a95ca41c7b511f5f04097d286
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08334295B2

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