반응 #7927

ord-81064133f67440459d71cf2f2f14c79e

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added over 2 minutes
  2. 2
    온도The mixture warmed during the addition
  3. 3
    여과filtered
  4. 4
    기타to remove the catalyst
  5. 5
    기타evaporated under vacuum
  6. 6
    기타The residue was partitioned between EtOAc (500 mL) and water (500 mL)
  7. 7
    세척The organic phase was washed with water (500 mL) and brine (100 mL)
  8. 8
    건조dried over MgSO4
  9. 9
    여과filtered
  10. 10
    기타evaporated under vacuum to an oil (33.5 g)
  11. 11
    기타The crude product was purified by column chromatography on EM silica gel 60 (230-400 mesh, 670 g)
  12. 12
    세척eluting first with CH2Cl2

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087599B2uspto-grants-2006_08