Water → 3-Methoxy-2-nitroaniline

HRID 422312

반응식

HRID 422312 반응식
C([N:3](CC)CC)C.P(N=[N+]=[N-])(OC1C=CC=CC=1)(OC1C=CC=CC=1)=O.[CH3:27][O:28][C:29]1[C:30]([N+:38]([O-:40])=[O:39])=[C:31]([CH:35]=[CH:36][CH:37]=1)C(O)=O.O>C1(C)C=CC=CC=1>[CH3:27][O:28][C:29]1[C:30]([N+:38]([O-:40])=[O:39])=[C:31]([NH2:3])[CH:35]=[CH:36][CH:37]=1

참가 물질

6

반응물 4

HCID 962WaterHCID 8471TriethylamineHCID 786323-Methoxy-2-nitrobenzoic acidHCID 123414Diphenylphosphoryl azide

생성물 1

HCID 104647003-Methoxy-2-nitroaniline수율 35%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

Triethylamine (6.29 mL) and diphenyl azidophosphate (6.66 mL, 30.1 mmol) were added to a suspension of 3-methoxy-2-nitrobenzoic acid (3.06 g, 15.2 mmol) in toluene (50 mL). The reaction mixture was stirred under reflux for 2 hours, water (10 mL) was added and it was stirred overnight under reflux. After evaporation of the solvent, the residue was dissolved in AcOEt and the resulting solution was filtered through celite. The organic phase was washed with saturated solution of NaHCO3, brine, dried over MgSO4, filtered and evaporated. The crude residue was purified by flash chromatography (cyclohexane/AcOEt 4:1) to yield 900 mg (5.35 mmol, 35%) of 3-methoxy-2-nitrophenylamine as a yellow solid.

후처리

  1. temperatureunder reflux for 2 hours
  2. stirringit was stirred overnight
  3. temperatureunder reflux
  4. customAfter evaporation of the solvent
  5. dissolutionthe residue was dissolved in AcOEt
  6. filtrationthe resulting solution was filtered through celite
  7. washThe organic phase was washed with saturated solution of NaHCO3, brine
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. customevaporated
  11. customThe crude residue was purified by flash chromatography (cyclohexane/AcOEt 4:1)

출처 및 근거

ORD 기록
ord-02c42d74a1fb4ea68414fbb86b725ab4
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08101637B2

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