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Bromine → Pentane

HRID 1436161
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반응식

HRID 1436161 반응식
[Br:1]Br.[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10](=[O:20])[CH2:11][C:12]2[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=2[Cl:19])=[CH:6][CH:5]=1>ClCCl>[CH3:6][CH2:5][CH2:4][CH2:9][CH3:8].[Br:1][CH:11]([C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=1[Cl:19])[C:10]([C:7]1[CH:8]=[CH:9][C:4]([Cl:3])=[CH:5][CH:6]=1)=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24408BromineHCID 5872691-(4-Chlorophenyl)-2-(2,4-dichlorophenyl)ethanone

생성물 2

HCID 8003Pentane수율 94%HCID 11164841HCID 11164841, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

2.5 ml of bromine are added dropwise to a solution of 1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)ethanone in dichloromethane (200 ml). The mixture is stirred for 4 hours at room temperature. The reaction medium is washed with water, with saturated aqueous NaHCO3 solution and then with aqueous NH4Cl solution. The organic phase is dried over Na2SO4, filtered and evaporated to dryness. The expected product is precipitated from pentane (yield=94%).

후처리

  1. washThe reaction medium is washed with water, with saturated aqueous NaHCO3 solution
  2. dry with materialThe organic phase is dried over Na2SO4
  3. filtrationfiltered
  4. customevaporated to dryness

출처 및 근거

ORD 기록
ord-1c979a0d0a1b4fe18b1415efcb1f1c11
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07618991B2

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