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1,3-Dichlorobenzene → (2-Chloro-5-nitrophenyl)(2,4-dichlorophenyl)methanone

HRID 1111347
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인쇄 미리보기

반응식

HRID 1111347 반응식
[Cl-].[Al+3].[Cl-].[Cl-].[Cl:5][C:6]1[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][C:7]=1[C:8](Cl)=[O:9].[Cl:18][C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([Cl:25])[CH:20]=1>ClCCl>[Cl:5][C:6]1[CH:14]=[CH:13][C:12]([N+:15]([O-:17])=[O:16])=[CH:11][C:7]=1[C:8]([C:22]1[CH:23]=[CH:24][C:19]([Cl:18])=[CH:20][C:21]=1[Cl:25])=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 109431,3-DichlorobenzeneHCID 117637Benzoyl chloride, 2-chloro-5-nitro-HCID 6451240Aluminum(III) Chloride

생성물 1

HCID 15072475(2-Chloro-5-nitrophenyl)(2,4-dichlorophenyl)methanone

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
80 °C

실험 절차

6 g of aluminium chloride are added to 5 g of 2-chloro-5-nitrobenzoyl chloride in 60 ml of dichloromethane, and 30 ml of 1,3-dichlorobenzene are then added dropwise. The reaction medium is heated for 2 hours at 80° C. and then cooled, and poured onto crushed ice. After extracting with dichloromethane, washing with water and drying over sodium sulphate, the organic phase is evaporated to dryness under vacuum and the crystalline residue is recrystallized in cyclohexane (3.6 g).

후처리

  1. additionare then added dropwise
  2. temperaturecooled
  3. additionpoured
  4. customonto crushed ice
  5. extractionAfter extracting with dichloromethane
  6. washwashing with water
  7. dry with materialdrying over sodium sulphate
  8. customthe organic phase is evaporated to dryness under vacuum
  9. customthe crystalline residue is recrystallized in cyclohexane (3.6 g)

출처 및 근거

ORD 기록
ord-0d56004845d840a3ab249254ecea94eb
출처 데이터셋
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04980349

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