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Water → 3-Chloro-2'-fluoro-2-hydroxy-4-methoxybenzophenone

HRID 568666
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반응식

HRID 568666 반응식
C[O:2][C:3]1[CH:10]=[CH:9][CH:8]=[C:5]([O:6][CH3:7])[C:4]=1[Cl:11].[F:12][C:13]1[CH:21]=[CH:20][CH:19]=[CH:18][C:14]=1[C:15](Cl)=[O:16].[Al+3].[Cl-].[Cl-].[Cl-].O>ClC(Cl)C>[Cl:11][C:4]1[C:3]([OH:2])=[C:10]([CH:9]=[CH:8][C:5]=1[O:6][CH3:7])[C:15]([C:14]1[CH:18]=[CH:19][CH:20]=[CH:21][C:13]=1[F:12])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 98082-Fluorobenzoyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 130157172-Chloro-1,3-dimethoxybenzene

생성물 1

HCID 130157183-Chloro-2'-fluoro-2-hydroxy-4-methoxybenzophenone

시약·촉매·용매 1

HCID 63651,1-Dichloroethane용매

실험 절차

2-chlororesorcinol dimethyl ether (22.0 g) and o-fluorobenzoyl chloride (20.2 g) are dissolved in 250 ml of dichloroethane, chilled in an ice bath and treated with AlCl3 (18.6 g). Fifteen minutes after the addition is complete, the reaction is heated to reflux for 30 minutes. It is poured into H2O and extracted with ethylacetate. Evaporation and trituration with hexane gives 3-chloro-2'-fluoro-2-hydroxy-4-methoxybenzophenone, mp 132°-133° C.

후처리

  1. temperaturechilled in an ice bath
  2. additionFifteen minutes after the addition
  3. temperaturethe reaction is heated
  4. temperatureto reflux for 30 minutes
  5. extractionextracted with ethylacetate
  6. customEvaporation and trituration with hexane

출처 및 근거

ORD 기록
ord-e22f11222ac44074a7fb3bca009e012a
출처 데이터셋
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04728662

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