Reaktion #2439510
ord-5d1df5c8071747c79535c090d10c0075
Reaktionsgleichung
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeUpon confirmation of full consumption of the raw material by thin-layer chromatography (eluent
- 2workup.ADDITIONa 5:1 mixture of n-hexane and ether), the
- 3Sonstigebubbling of hydrogen chloride gas
- 4workup.ADDITIONWater was added to the reaction mixture
- 5Extraktionfollowed by extraction of the resultant mixture
- 6Extraktionfollowed by extraction of the resultant mixture with ether
- 7WaschenAfter the resultant ether solution was washed with water
- 8Trocknena saturated aqueous solution of sodium hydrogencarbonate and water successively, the ether solution was dried over anhydrous magnesium sulfate
- 9Einengenconcentrated under reduced pressure
- 10SonstigeThe residue was purified by column chromatography on silica gel (eluent
- 11workup.ADDITIONa 10:1 mixture of n-hexane and ether)
Vorschrift
Dissolved in 80 ml of methanol was 12 g of 2-n-butyl-3-(3,4-methylenedioxyphenyl)acrylaldehyde, into which hydrogen chloride gas was blown under ice-salt cooling. Upon confirmation of full consumption of the raw material by thin-layer chromatography (eluent: a 5:1 mixture of n-hexane and ether), the bubbling of hydrogen chloride gas was stopped. Water was added to the reaction mixture, followed by extraction of the resultant mixture, followed by extraction of the resultant mixture with ether. After the resultant ether solution was washed with water, a saturated aqueous solution of sodium hydrogencarbonate and water successively, the ether solution was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: a 10:1 mixture of n-hexane and ether) to give 11.4 g of 2-n-butyl-3-methoxy-5,6-methylenedioxyindene as an oily substance (yield: 90%).