반응 #1766

ord-b4fd402e735143d2ba1df2c8a9a0fe8f

반응 방정식

COC(=O)c1ccc(O)cc1O
methyl 2,4-dihydroxybenzoate
O=C([O-])[O-].[K+].[K+]
K2CO3
BrCc1ccccc1
benzyl bromide
COC(=O)c1ccc(OCc2ccccc2)cc1O
methyl 4-benzyloxy-2-hydroxybenzoate

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The reaction solution was filtered through celite
  2. 2
    workup.DISSOLUTIONThe crude oil was dissolved in EtOAc (1000 mL)
  3. 3
    세척washed with water (250 mL), and saturated aqueous NaHCO3 (500 mL)
  4. 4
    건조The EtOAc layer was dried (MgSO4)
  5. 5
    여과filtered
  6. 6
    기타the EtOAc was removed under reduced pressure
  7. 7
    기타The crude product was purified by pressurized silica gel column chromatography
  8. 8
    기타Evaporation of the hexanes

실험 절차

To a stirred, 0° C. solution of methyl 2,4-dihydroxybenzoate (50 g, 300 mmol) in acetone (1000 mL) was added K2CO3 (150 g, 1000 mmol) and benzyl bromide (330 mmol, 39 mL). The solution was allowed to warm to ambient temperature over 48 h. The reaction solution was filtered through celite and the acetone solution stripped down under reduced pressure. The crude oil was dissolved in EtOAc (1000 mL) and washed with water (250 mL), and saturated aqueous NaHCO3 (500 mL). The EtOAc layer was dried (MgSO4), filtered, and the EtOAc was removed under reduced pressure. The crude product was purified by pressurized silica gel column chromatography using 5:1 hexanes:EtOAc. Evaporation of the hexanes:EtOAc mixture gave the desired methyl 4-benzyloxy-2-hydroxybenzoate as a white powder.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05726172uspto-grants-1998_03