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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → {[5-Chloro-4'-(ethylthio)biphenyl-2-yl]oxy}acetic acid

HRID 1694682
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인쇄 미리보기

반응식

HRID 1694682 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:17][CH2:18][C:19]([O:21]C(C)(C)C)=[O:20])=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([S:14][CH2:15][CH3:16])=[CH:10][CH:9]=2)[CH:7]=1.FC(F)(F)C(O)=O>C(Cl)Cl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:17][CH2:18][C:19]([OH:21])=[O:20])=[C:6]([C:8]2[CH:9]=[CH:10][C:11]([S:14][CH2:15][CH3:16])=[CH:12][CH:13]=2)[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 86609213tert-Butyl {[5-chloro-4'-(ethylthio)biphenyl-2-yl]oxy}acetate

생성물 1

HCID 11163081{[5-Chloro-4'-(ethylthio)biphenyl-2-yl]oxy}acetic acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

The title compound was prepared by stirring a mixture of the product from step (ii) (0.3 g) and trifluoroacetic acid (4 ml) in DCM (10 ml) at RT for 5 h. The solvent was evaporated under reduced pressure, the residue triturated with diethylether then purified by reverse phase HPLC. Yield 0.106 g

후처리

  1. customThe solvent was evaporated under reduced pressure
  2. customthe residue triturated with diethylether
  3. customthen purified by reverse phase HPLC

출처 및 근거

ORD 기록
ord-38685364f43447d9b553ecdadb2461d0
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08158820B2

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