HRID7831

反应详情

EQUATION

反应方程式

HRID 7831 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 5-methoxy-1-indanone (25.0 g, 154 mmol), 85% KOH (2.03 g, 30.8 mmol), 10% palladium on activated carbon (2 g), and ethanol (150 mL) was placed under a hydrogen atmosphere and stirred while butyraldehyde (16.7 mL, 185 mmol) was added over 2 minutes. The mixture warmed during the addition. The resulting mixture was hydrogenated at room temperature for 3 hours, then filtered to remove the catalyst. The filtrate was acidified with 2N HCl (15.4 mL, 30.8 mmol) and evaporated under vacuum. The residue was partitioned between EtOAc (500 mL) and water (500 mL). The organic phase was washed with water (500 mL) and brine (100 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (33.5 g). The crude product was purified by column chromatography on EM silica gel 60 (230-400 mesh, 670 g), eluting first with CH2Cl2 and then with 5% EtOAc in CH2Cl2, to afford 2-butyl-5-methoxy-1-indanone (17.9 g) as an oil.

WORKUP

后处理

  1. additionwas added over 2 minutes
  2. temperatureThe mixture warmed during the addition
  3. filtrationfiltered
  4. customto remove the catalyst
  5. customevaporated under vacuum
  6. customThe residue was partitioned between EtOAc (500 mL) and water (500 mL)
  7. washThe organic phase was washed with water (500 mL) and brine (100 mL)
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. customevaporated under vacuum to an oil (33.5 g)
  11. customThe crude product was purified by column chromatography on EM silica gel 60 (230-400 mesh, 670 g)
  12. washeluting first with CH2Cl2