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Trifluoroacetic anhydride → 5-Fluoro-3-(thiazol-2-ylcarbonyl)thiophenol

HRID 260432
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인쇄 미리보기

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HRID 260432 반응식
C[S:2]([C:4]1[CH:5]=[C:6]([C:11]([C:13]2[S:14][CH:15]=[CH:16][N:17]=2)=[O:12])[CH:7]=[C:8]([F:10])[CH:9]=1)=O.C(OC(C(F)(F)F)=O)(C(F)(F)F)=O>ClC(Cl)C>[F:10][C:8]1[CH:7]=[C:6]([C:11]([C:13]2[S:14][CH:15]=[CH:16][N:17]=2)=[O:12])[CH:5]=[C:4]([SH:2])[CH:9]=1
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참가 물질

4

반응물 2

HCID 9845Trifluoroacetic anhydrideHCID 19426964HCID 19426964, 화합물

생성물 1

HCID 194270015-Fluoro-3-(thiazol-2-ylcarbonyl)thiophenol

시약·촉매·용매 1

HCID 63651,1-Dichloroethane용매

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온도
80 °C

실험 절차

To a solution of the sulfoxide from Step 2 (0.35 g, 1.29 mmol) in dichloroethane (2.6 mL) was added TFAA (2.6 mL). The mixture was stirred at 80° C. for 0.5 h, cooled and evaporated. The residue was dissolved in MeOH: Et3N (1:1, 5 mL). The solvent was evaporated and taken up again in MeOH/Et3N. After evaporation of the solvent and chromatography using hexane:EtOAc (70:30) 0.28 g of the title compound was obtained.

후처리

  1. temperaturecooled
  2. customevaporated
  3. dissolutionThe residue was dissolved in MeOH: Et3N (1:1, 5 mL)
  4. customThe solvent was evaporated
  5. customAfter evaporation of the solvent and chromatography
  6. customwas obtained

출처 및 근거

ORD 기록
ord-0cee7e937b734a9aba588270a04d5814
출처 데이터셋
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05527827

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