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N-bromobutanimide → Methyl alpha-bromo-2-chlorophenylacetate

HRID 224293
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HRID 224293 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([O:11][CH3:12])=[O:10].[Br:13]N1C(=O)CCC1=O>Br.C(Cl)(Cl)(Cl)Cl>[Br:13][CH:8]([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[Cl:1])[C:9]([O:11][CH3:12])=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 67184N-bromobutanimideHCID 93683Methyl (2-chlorophenyl)acetate

생성물 1

HCID 10730282Methyl alpha-bromo-2-chlorophenylacetate

시약·촉매·용매 2

HCID 260Hydrogen Bromide촉매HCID 5943Carbon Tetrachloride용매

실험 절차

A stirred mixture of 36.9 g of methyl o-chlorophenylacetate, 36.0 g of N-bromosuccinimide, and 2 drops of 48% hydrobromic acid in 500 ml of carbon tetrachloride is refluxed for 20 hours and then filtered through magnesium silicate. Evaporation under reduced pressure gives methyl α-bromo-o-chlorophenylacetate as a straw-colored liquid.

후처리

  1. temperatureis refluxed for 20 hours
  2. filtrationfiltered through magnesium silicate
  3. customEvaporation under reduced pressure

출처 및 근거

ORD 기록
ord-0727808507f14d0a92aabc1d744f2376
출처 데이터셋
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04231935

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