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Bromine → 5-Bromo-2-hydroxy-3-(trifluoromethyl)pyridine

HRID 1844704
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HRID 1844704 반응식
[F:1][C:2]([F:11])([F:10])[C:3]1[C:4](=[O:9])[NH:5][CH:6]=[CH:7][CH:8]=1.CC([O-])=O.[Na+].[Br:17]Br>CC(O)=O>[Br:17][C:7]1[CH:8]=[C:3]([C:2]([F:1])([F:10])[F:11])[C:4](=[O:9])[NH:5][CH:6]=1
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참가 물질

5

반응물 3

HCID 24408BromineHCID 517045Sodium AcetateHCID 36784112(1H)-Pyridinone, 3-(trifluoromethyl)-

생성물 1

HCID 134917805-Bromo-2-hydroxy-3-(trifluoromethyl)pyridine

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
80 °C

실험 절차

To a solution of 3-(trifluoromethyl)pyridin-2(1H)-one (25.0 g, 0.15 mol) in AcOH (300 mL) were added NaOAc (15.1 g, 0.18 mol) and dropwise Br2 (8.6 mL, 0.17 mol). Then the mixture was stirred at 80° C. overnight, concentrated, diluted with sat aq. NaHCO3 and extracted with EtOAc twice. The combined organic layers were washed with brine, dried over Na2SO4, filtered, concentrated and purified by CC (PE/EA=7/2) to give compound P45a (29.7 g, 80%) as a white solid.

후처리

  1. concentrationconcentrated
  2. additiondiluted with sat aq. NaHCO3
  3. extractionextracted with EtOAc twice
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. custompurified by CC (PE/EA=7/2)
  9. customto give compound P45a (29.7 g, 80%) as a white solid

출처 및 근거

ORD 기록
ord-4ef11352619d4c119d2ddfcb7a71b57f
출처 데이터셋
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08946446B2

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