Reaktion #2061639
ord-e3c9db2edbc143e4974f6f29bcc397ee
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturat reflux temperature for 2 hours
- 2Sonstige30 minutes
- 3Einengenconcentrated in vacuo
- 4Sonstigeto give a liquid
- 5SonstigeThe liquid is partitioned between methylene chloride and 5% sodium bicarbonate solution
- 6SonstigeThe layers are separated
- 7Extraktionthe aqueous layer is extracted with methylene chloride
- 8Trocknenthe combined methylene chloride extracts are dried over anhydrous magnesium sulfate
- 9Einengenconcentrated in vacuo
- 10Sonstigeto give an oil
- 11SonstigeThe oil is chromatographed
Vorschrift
A solution of 5-formyl-2,3 pyridinedicarboxylic acid, dimethyl ester, 5-dimethyl acetal (1.3 g, 0.0048 mol), a catalytic amount of p-toluenesulfonic acid, 1,4-butanediol and toluene is heated at reflux temperature for 2 hours and 30 minutes. The reaction mixture is cooled to room temperature, made basic with sodium bicarbonate and concentrated in vacuo to give a liquid. The liquid is partitioned between methylene chloride and 5% sodium bicarbonate solution. The layers are separated and the aqueous layer is extracted with methylene chloride, the combined methylene chloride extracts are dried over anhydrous magnesium sulfate and concentrated in vacuo to give an oil. The oil is chromatographed using silica gel and hexanes/ethyl acetate (2:1 to 1:1) as eluant to give the title compound as a clear oil (0.88 g, 62%), identified by IR and NMR spectral analyses.