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3,4-Dichlorobenzotrifluoride → 3-(2'-Chloro-4-trifluoromethylphenoxy)-6-chlorothioanisole

HRID 1702740
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인쇄 미리보기

반응식

HRID 1702740 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[S:9][CH3:10].[Cl:11][C:12]1[CH:13]=[C:14]([C:19]([F:22])([F:21])[F:20])[CH:15]=[CH:16][C:17]=1Cl.[OH-].[Na+]>CS(C)=O>[Cl:11][C:12]1[CH:13]=[C:14]([C:19]([F:20])([F:21])[F:22])[CH:15]=[CH:16][C:17]=1[O:8][C:5]1[CH:4]=[C:3]([S:9][CH3:10])[C:2]([Cl:1])=[CH:7][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 94813,4-DichlorobenzotrifluorideHCID 14798Sodium HydroxideHCID 218771864-Chloro-3-(methylthio)phenol

생성물 1

HCID 205247373-(2'-Chloro-4-trifluoromethylphenoxy)-6-chlorothioanisole수율 80.1%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

50 g of 4-chloro-3-methylmercaptophenol, 62 g of 3,4-dichlorobenzotrifluoride and 12 g of sodium hydroxide are stirred in 150 ml of dimethyl sulphoxide for 6 hours at 142° C. The reaction mixture is then poured onto ice and extracted with toluene. Distillation of the organic phase yields 81 g of 3-(2'-chloro-4-trifluoromethylphenoxy)-6-chlorothioanisole with a boiling point of 158° C./0.4 mbar.

후처리

  1. additionThe reaction mixture is then poured onto ice
  2. extractionextracted with toluene
  3. distillationDistillation of the organic phase

출처 및 근거

ORD 기록
ord-b17eee9299504d18a4c2c398e032ba2d
출처 데이터셋
uspto-grants-1982_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04349377

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