반응 #7927
ord-81064133f67440459d71cf2f2f14c79e
용매
반응 조건
후처리
- 1workup.ADDITIONwas added over 2 minutes
- 2온도The mixture warmed during the addition
- 3여과filtered
- 4기타to remove the catalyst
- 5기타evaporated under vacuum
- 6기타The residue was partitioned between EtOAc (500 mL) and water (500 mL)
- 7세척The organic phase was washed with water (500 mL) and brine (100 mL)
- 8건조dried over MgSO4
- 9여과filtered
- 10기타evaporated under vacuum to an oil (33.5 g)
- 11기타The crude product was purified by column chromatography on EM silica gel 60 (230-400 mesh, 670 g)
- 12세척eluting 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.