Sodium Sulfate → 5-Bromo-2-(difluoromethoxy)pyridine

HRID 1095832노트

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HRID 1095832 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5](=[O:8])[NH:6][CH:7]=1.S([O-])([O-])(=O)=O.[Na+].[Na+].FS([C:20]([F:25])([F:24])C(O)=O)(=O)=O.C(=O)([O-])O.[Na+]>C(#N)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:8][CH:20]([F:25])[F:24])=[N:6][CH:7]=1

참가 물질

6

실험 절차

5-Bromopyridin-2(1H)-one (17.4 g, 100 mmol) was mixed with sodium sulfate (1.42 g, 10 mmol) and 2-(fluorosulfonyl)difluoroacetic acid (11.4 ml, 100 mmol) in acetonitrile, and stirred overnight at room temperature. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction solution, and the solvent was concentrated under reduced pressure. The residue was dissolved in diethyl ether, washed with saturated saline, the organic layer was dried with sodium sulfate, and the solvent was evaporated off under reduced pressure. The residue was purified through silica gel column chromatography (eluate: ethyl acetate/hexane=20/80 to 50/50) to obtain the entitled compound (18.75 g, 84%) as a pale yellow oily substance.

후처리

  1. concentrationthe solvent was concentrated under reduced pressure
  2. dissolutionThe residue was dissolved in diethyl ether
  3. washwashed with saturated saline
  4. dry with materialthe organic layer was dried with sodium sulfate
  5. customthe solvent was evaporated off under reduced pressure
  6. customThe residue was purified through silica gel column chromatography (eluate: ethyl acetate/hexane=20/80 to 50/50)

출처 및 근거

ORD 기록
ord-eb6264440c2948f493d2415e44d2b11b
출처 데이터셋
uspto-grants-2012_03
특허 번호
US08138206B2

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