m-Chloroperbenzoic acid → 2-Chloro-4-methylpyridine 1-oxide

HRID 37852

반응식

HRID 37852 반응식
ClC1C=CC=C(C(OO)=[O:9])C=1.[Cl:12][C:13]1[CH:18]=[C:17]([CH3:19])[CH:16]=[CH:15][N:14]=1>C(Cl)(Cl)Cl>[Cl:12][C:13]1[CH:18]=[C:17]([CH3:19])[CH:16]=[CH:15][N+:14]=1[O-:9]

참가 물질

4

실험 절차

40% meta-chloroperbenzoic acid (13.5 g, 31.4 mmol) was added at ambient temperature to a solution of 2-chloro-4-methyl-pyridine (2.0 g, 1.5 mmol) in chloroform (20 mL) and heated at reflux for 24 h. After allowing to cool, the mixture was washed with water followed by sodium bicarbonate solution. The separated organic phase was further washed with water and brine, dried over anhydrous sodium sulfate and concentrated to give a residue which was purified by column chromatography over silica gel (60-120 mesh) using 10% methanol in ethyl acetate as eluent to afford 2-chloro-4-methyl-pyridine 1-oxide (1.0 g, 45%) as a deep brown oily liquid.

후처리

  1. temperatureheated
  2. temperatureat reflux for 24 h
  3. temperatureto cool
  4. washthe mixture was washed with water
  5. washThe separated organic phase was further washed with water and brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated
  8. customto give a residue which
  9. customwas purified by column chromatography over silica gel (60-120 mesh)

출처 및 근거

ORD 기록
ord-c2ddec53bd744cd7b5a933c42f3d5d64
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08524705B2

연결된 노트

불러오는 중…