반응 #49534

ord-98ca684b2d7041bc8d3afabb280632b7

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooling
  2. 2
    온도cooling
  3. 3
    workup.STIRRINGstirred at room temperature for 1.5 hours
  4. 4
    workup.STIRRINGstirred at room temperature for 18 hours
  5. 5
    기타The solvent was evaporated under reduced pressure
  6. 6
    workup.ADDITIONthe residue was added with 4 mol/L hydrochloric acid and water
  7. 7
    추출by extracting with ethyl acetate
  8. 8
    세척The organic layer was washed with saturated brine
  9. 9
    건조dried over anhydrous sodium sulfate
  10. 10
    기타The solvent was evaporated under reduced pressure

실험 절차

3-Chloro-4-hydroxybenzoic acid 0.5 hydrate (2.00 g, 11.6 mmol) was suspended in dichloromethane (50 mL), and the suspension was added with diisopropylethylamine (8.10 mL, 46.5 mmol) and chloromethyl methyl ether (1.80 mL, 23.7 mmol), under ice-cooling. The reaction mixture was warmed to room temperature and stirred for 1.5 hours. The reaction mixture was added with chloromethyl methyl ether (0.45 mL, 5.92 mmol) under ice-cooling, and stirred at room temperature for 1.5 hours. The reaction mixture was added with methanol (100 mL) and 4 mol/L aqueous potassium hydroxide solution (50 mL) and stirred at room temperature for 18 hours. The solvent was evaporated under reduced pressure, and the residue was added with 4 mol/L hydrochloric acid and water, followed by extracting with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to obtain 3-chloro-4-methoxymethoxybenzoic acid (2.39 g, yield 95%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745641B2uspto-grants-2010_06