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Bromine → 1-Bromo-5-chloro-1-(4-chlorophenoxy)-3,3-dimethylpentan-2-one

HRID 464392
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인쇄 미리보기

반응식

HRID 464392 반응식
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][CH2:7][C:8](=[O:15])[C:9]([CH3:14])([CH3:13])[CH2:10][CH2:11][Cl:12])=[CH:4][CH:3]=1.[Br:18]Br>C(Cl)Cl>[Br:18][CH:7]([O:6][C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:17][CH:16]=1)[C:8](=[O:15])[C:9]([CH3:13])([CH3:14])[CH2:10][CH2:11][Cl:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24408BromineHCID 132542805-Chloro-1-(4-chlorophenoxy)-3,3-dimethylpentan-2-one

생성물 1

HCID 132542811-Bromo-5-chloro-1-(4-chlorophenoxy)-3,3-dimethylpentan-2-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

136 g (0.5 mol) of 1-(4-chlorophenoxy)-5-chloro-3,3-dimethyl-2-pentanone are dissolved in 1000 ml of methylene chloride. 79.9 g (1 mol) of bromine are added dropwise at room temperature such that the solution is always decolorized. The reaction mixture is then subsequently stirred at room temperature for 1 hour and is concentrated by distilling off the solvent. A quantitative yield, that is to say 177 g, of 1-bromo-1-(4-chlorophenoxy)-5-chloro-3,3-dimethyl-2-pentanone is obtained, and is further reacted directly. ##STR29##

후처리

  1. concentrationis concentrated
  2. distillationby distilling off the solvent

출처 및 근거

ORD 기록
ord-c82b09cc2ed9450597913b666c2b12ba
출처 데이터셋
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04547515

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