Phosphorus oxybromide → 2-Bromo-4-methyl-5-nitropyridine

HRID 751618

반응식

HRID 751618 반응식
O[C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][N:3]=1.P(Br)(Br)([Br:14])=O>ClC(Cl)C>[Br:14][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][N:3]=1

참가 물질

4

실험 절차

To a suspension of 2-hydroxy-4-methyl-5-nitropyridine (1 g, 6.5 mmol) in dichloroethane (10 mL) was added a solution of phosphorus oxybromide (2.8 g, 9.7 mmol) in dichloroethane (10 mL). The reaction mixture was heated under reflux for 4 h, then cooled to rt and quenched with water (40 mL). The layers were separated and the aqueous layer extracted into dichloromethane (2×3 mL). The combined organics were dried (MgSO4), concentrated in vacuo and chromatographed on silica gel eluting with dichloromethane to give the title compound as a pale yellow solid. δH (CDCl3): 2.63 (3H, s), 7.52 (1H, s), 8.96 (1H, s).

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureunder reflux for 4 h
  3. customquenched with water (40 mL)
  4. customThe layers were separated
  5. extractionthe aqueous layer extracted into dichloromethane (2×3 mL)
  6. dry with materialThe combined organics were dried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. customchromatographed on silica gel eluting with dichloromethane

출처 및 근거

ORD 기록
ord-a5162261122a479fb38bdaf3ff175659
출처 데이터셋
uspto-grants-2008_07
특허 번호
US07405210B2

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