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Hydrochloric Acid → 3-Chloro-2-hydroxy-4-methoxy-2'-trifluoromethylbenzophenone

HRID 652907
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HRID 652907 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]([F:24])([F:23])[C:14]1[CH:22]=[CH:21][CH:20]=[CH:19][C:15]=1[C:16](Cl)=[O:17].Cl>ClCCCl>[Cl:11][C:4]1[C:3]([OH:2])=[C:10]([CH:9]=[CH:8][C:5]=1[O:6][CH3:7])[C:16]([C:15]1[CH:19]=[CH:20][CH:21]=[CH:22][C:14]=1[C:13]([F:12])([F:23])[F:24])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 675612-(Trifluoromethyl)benzoyl chlorideHCID 130157172-Chloro-1,3-dimethoxybenzene

생성물 1

HCID 140125683-Chloro-2-hydroxy-4-methoxy-2'-trifluoromethylbenzophenone

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

To a solution of 1.7 g of 2-chlororesorcinol dimethyl ether and 2.08 g of o-trifluoromethyl benzoyl chloride in 50 ml of 1,2-dichloroethane at 5°-7° C., 1.6 g of ferric chloride is added gradually. The mixture is brought to room temperature and allowed to stand 18 hours. The reaction mixture is refluxed 30 minutes and poured into 5% HCl and ice. The aqueous phase is extracted with additional organic solvent. The combined organic extracts are washed with water, dried over Na2SO4 and evaporated to give 3-chloro-2-hydroxy-4-methoxy-2'-trifluoromethylbenzophenone, mp 101°-102° C.

후처리

  1. customis brought to room temperature
  2. temperatureThe reaction mixture is refluxed 30 minutes
  3. extractionThe aqueous phase is extracted with additional organic solvent
  4. washThe combined organic extracts are washed with water
  5. dry with materialdried over Na2SO4
  6. customevaporated

출처 및 근거

ORD 기록
ord-2e7699a6b65c43ffa16b18d6d6e9ef58
출처 데이터셋
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04673746

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