Reaktion #362036
ord-b7b5d8a724604f80800b2e11dc4c62c3
Reaktionsgleichung
Edukte
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1TemperaturThe mixture is heated further at 40° C. for 61 hours
- 2Einengenconcentrated at 60° C./5 mm
- 3Sonstigeto leave a greenish oil that
- 4Filtrationfiltered through a pad of silica gel (230-400 mesh)
- 5workup.ADDITIONThe filtrate is diluted with additional ethyl acetate
- 6Waschenthe organic phase is washed with water
- 7Sonstigedried
- 8Einengenconcentrated to an oil
- 9workup.DISTILLATIONThe oil is distilled, with material
- 10Sonstigecollected in the 80°-95° C./0.14 mm ranger
Vorschrift
2-Ethenyl-3-pyridinecarboxylic acid, methyl ester (12) is prepared as follows: a mixture of 19.7 g (115 mmol) of 2-chloro-3-pyridinecarboxylic acid, methyl ester (11), 38.3 g (120.8 mmol) of vinyltributyltin, 1.48 g (2.1 mmol) of bis(triphenylphosphine)palladium (II) chloride 100 mg of 2,6-ditertbutyl-4-methylphenol, and 250 mL of N,N-dimethylformamide is stirred at 55° C. for 7 hours, then treated with 1.63 g 15.1 mmol) of additional vinyltributyltin and 1 g of palladium catalyst. The mixture is heated further at 40° C. for 61 hours, then concentrated at 60° C./5 mm to leave a greenish oil that is dissolved in ethyl acetate and filtered through a pad of silica gel (230-400 mesh). The filtrate is diluted with additional ethyl acetate and the organic phase is washed with water, dried, and concentrated to an oil. The oil is distilled, with material collected in the 80°-95° C./0.14 mm ranger to leave 24.5 g of an oil that is ca. 75% product by GC. The oil is dissolved in dichloromethane:hexanes (1:1) and loaded onto an 8 x 15 cm of silica gel column (230-400 mesh). The column is eluted with the same solvent as above with 500 mL fractions collected. Product fractions are combined and carefully distilled at 65°-67° C./0.15 mm to leave 13.6 g of clear oil, >95% pure by GC, that is sufficiently pure to use directly in the next step.