HRID1511016

反应详情

EQUATION

反应方程式

HRID 1511016 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

POCl3 (12.9 ml, 141.2 mmol) was added to DMF (10.9 ml, 141.2 mmol) at 0° C. The reaction was immediately warmed to ambient temperature and stirred for 30 minutes. ((2,2-diethoxyethoxy)methyl)benzene (10.6 g, 47.1 mmol) was added as a solution in 80 mL of chloroform. The solution was stirred at 75° C. for 3.5 hours. The solution was cooled, poured over ice water, and neutralized with Na2CO3. The residue was extracted with chloroform and the organic layer was dried with Na2SO4 and concentrated. The residue was re-dissolved in MeOH (450 mL). NaOMe (25% in MeOH, 58 ml, 253 mmol) was added followed by 2-hydrazinylethanol (10.6 g, 139 mmol). The reaction stirred overnight at ambient temperature. The material was concentrated in vacuo followed by dilution with saturated NH4Cl solution. The material was extracted with EtOAc, dried (Mg2SO4), and concentrated. Flash chromatography gave 2-(4-(benzyloxy)-1H-pyrazol-1-yl)ethanol (1.81 g, 13% yield).

WORKUP

后处理

  1. stirringThe solution was stirred at 75° C. for 3.5 hours
  2. temperatureThe solution was cooled
  3. extractionThe residue was extracted with chloroform
  4. dry with materialthe organic layer was dried with Na2SO4
  5. concentrationconcentrated
  6. dissolutionThe residue was re-dissolved in MeOH (450 mL)
  7. stirringThe reaction stirred overnight at ambient temperature
  8. concentrationThe material was concentrated in vacuo
  9. extractionThe material was extracted with EtOAc
  10. dry with materialdried (Mg2SO4)
  11. concentrationconcentrated