Methanol → 2-(4-Methoxy-phenoxy)-5-nitro-benzoic acid methyl ester

HRID 47437노트

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HRID 47437 반응식
[CH3:1][O:2][C:3]1[CH:21]=[CH:20][C:6]([O:7][C:8]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][C:9]=2[C:10]([OH:12])=[O:11])=[CH:5][CH:4]=1.[CH3:22]O>S(=O)(=O)(O)O>[CH3:22][O:11][C:10](=[O:12])[C:9]1[CH:13]=[C:14]([N+:17]([O-:19])=[O:18])[CH:15]=[CH:16][C:8]=1[O:7][C:6]1[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:21][CH:20]=1

참가 물질

4

실험 절차

2-(4-Methoxy-phenoxy)-5-nitro-benzoic acid (2.5 g), (DE 2058295) in methanol (75 ml) containing conc. sulfuric acid (3 drops) was boiled for 16 h. Solvent was removed at reduced pressure, the residue dissolved in ethyl acetate and washed with aqueous sodium hydrogen carbonate. The organic phase was dried (Na2SO4) and solvent removed at reduced pressure to give 2-(4-methoxy-phenoxy)-5-nitro-benzoic acid methyl ester (2.50 g). m/z (API+): 304 (MH+).

후처리

  1. customSolvent was removed at reduced pressure
  2. dissolutionthe residue dissolved in ethyl acetate
  3. washwashed with aqueous sodium hydrogen carbonate
  4. dry with materialThe organic phase was dried (Na2SO4) and solvent
  5. customremoved at reduced pressure

출처 및 근거

ORD 기록
ord-fcd65e698cba4ce88f7661c0861eb09c
출처 데이터셋
uspto-grants-2004_03
특허 번호
US06699879B1

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