Chloromethyl Methyl Ether → 4-Formyl-3-methoxymethoxybenzoic acid

HRID 21250노트

반응식

HRID 21250 반응식
[CH:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][C:4]=1[OH:12])=[O:2].C(N(C(C)C)CC)(C)C.[CH3:22][O:23][CH2:24]Cl>ClCCl>[CH:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][C:4]=1[O:12][CH2:22][O:23][CH3:24])=[O:2]

참가 물질

5

실험 절차

4-Formyl-3-hydroxybenzoic acid (2.20 g, 13.2 mmol) was suspended in dichloromethane (40 mL), and the suspension was added with diisopropylethylamine (9.20 mL, 52.8 mmol) and chloromethyl methyl ether (2.01 mL, 26.5 mmol) under ice-cooling. Then, the reaction mixture was warmed to room temperature and stirred for 1 hour. The solvent was evaporated under reduced pressure and the residue was dissolved in methanol (40 mL), and the solution was added with 2 mol/L aqueous potassium hydroxide solution (40 mL), and stirred at room temperature for 1 hour. Methanol was evaporated under reduced pressure and the residue was added with 4 mol/L hydrochloric acid and water. The precipitated solid was collected by filtration and washed with water, followed by drying under reduced pressure to obtain 4-formyl-3-methoxymethoxybenzoic acid (2.21 g, yield 80%).

후처리

  1. temperaturecooling
  2. customThe solvent was evaporated under reduced pressure
  3. dissolutionthe residue was dissolved in methanol (40 mL)
  4. additionthe solution was added with 2 mol/L aqueous potassium hydroxide solution (40 mL)
  5. stirringstirred at room temperature for 1 hour
  6. customMethanol was evaporated under reduced pressure
  7. additionthe residue was added with 4 mol/L hydrochloric acid and water
  8. filtrationThe precipitated solid was collected by filtration
  9. washwashed with water
  10. customby drying under reduced pressure

출처 및 근거

ORD 기록
ord-8c84d9f0f0474201bd3b468686c19dd9
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07745641B2

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