Reacción #1552018
ord-5161a8ec092a415c91d1f5cfd3d86e73
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONwas dropped over an hour
- 2workup.STIRRINGThis solution was stirred for 2 hours
- 3workup.STIRRINGsubsequently further stirred at room temperature for 6 hours
- 4OtroThe resultant reaction solution
- 5Lavadowas rinsed with water
- 6Otrothe organic phase was then separated
- 7Secadodried over magnesium sulfate
- 8workup.DISTILLATIONthe solvent was distilled off
- 9OtroThe residue was purified by silica gel column chromatography with a methylene chloride/methanol (97/3) solvent mixture
Procedimiento
Ethylene glycol (15.6 g, 252 mmol) was dissolved in 100 mL of methylene chloride. To this solution, 3.49 g (44 mmol) of pyridine was added and the solution was cooled with ice water. To this solution being stirred, a solution containing 8.00 g (42 mmol) of 2-naphthalenecarbonyl chloride dissolved in 80 mL of methylene chloride was dropped over an hour. This solution was stirred for 2 hours and subsequently further stirred at room temperature for 6 hours. The resultant reaction solution was rinsed with water; the organic phase was then separated and dried over magnesium sulfate, and the solvent was distilled off. The residue was purified by silica gel column chromatography with a methylene chloride/methanol (97/3) solvent mixture serving as an eluent to provide 6.88 g of 2-naphthoic acid 2-hydroxyethyl ester.