Dimethylformamide → 5-Iodo-N,N-dimethyl-2-nitrobenzamide

HRID 423268노트

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HRID 423268 반응식
[I:1][C:2]1[CH:3]=[CH:4][C:5]([N+:11]([O-:13])=[O:12])=[C:6]([CH:10]=1)[C:7](O)=[O:8].C(Cl)(=O)C(Cl)=O.[CH3:20][N:21](C)[CH:22]=O>C(Cl)(Cl)Cl>[I:1][C:2]1[CH:3]=[CH:4][C:5]([N+:11]([O-:13])=[O:12])=[C:6]([CH:10]=1)[C:7]([N:21]([CH3:22])[CH3:20])=[O:8]

참가 물질

5

실험 절차

5-Iodo-2-nitrobenzoic acid (15.5 g) was dissolved in chloroform (30 mL). Oxalyl chloride (13.4 g) was added thereto at 0° C., and then DMF (dimethylformamide) (0.1 mL) was further added. The mixture was stirred at room temperature for 2 hours, and then concentrated. After addition of toluene to the residue, the mixture was further concentrated. A solution of the concentrated residue in ethyl acetate (60 mL) was added dropwise to a mixed solution of 50% (w/w) aqueous dimethylamine (7.5 mL) saturated aqueous sodium bicarbonate (60 mL), and toluene (60 mL) under stirring and ice-cooling. The reaction solution was diluted with ethyl acetate, washed with saturated aqueous sodium bicarbonate and saturated brine, and concentrated to give the title compound (15.3 g).

후처리

  1. concentrationconcentrated
  2. additionAfter addition of toluene to the residue
  3. concentrationthe mixture was further concentrated
  4. additionA solution of the concentrated residue in ethyl acetate (60 mL) was added dropwise to a mixed solution of 50% (w/w) aqueous dimethylamine (7.5 mL) saturated aqueous sodium bicarbonate (60 mL), and toluene (60 mL)
  5. stirringunder stirring
  6. temperatureice-cooling
  7. additionThe reaction solution was diluted with ethyl acetate
  8. washwashed with saturated aqueous sodium bicarbonate and saturated brine
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-da66ac0fccd34ec1a7dd9fdb3645536d
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08101774B2

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