Reacción #47242
ord-e6036ef11aa9408e8fa664960532b4d3
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONAfter addition
- 2workup.ADDITIONwas added in small portions
- 3Otrotransferred to a separatory funnel
- 4Otrothe layers separated
- 5Lavadoby washing the aqueous layer with petroleum ether (2×50 mL)
- 6LavadoThe combined petroleum ether extracts were washed with a 20% potassium carbonate solution
- 7Secadodried over magnesium sulfate
- 8ConcentraciónThe combined organic layers were concentrated
- 9Otroto give a yellow oil
- 10workup.DISTILLATIONDistillation of the residue
Procedimiento
To a stirred mixture of ethyl acetoacetate (15.0 g, 0.12 mol) in petroleum ether (30 mL) under a nitrogen atmosphere was added phosphorus pentachloride (12.7 g, 0.06 mol) gradually. After addition was complete the mixture was stirred at 25° C. for 1 h. Upon completion of the reaction water (50 mL) was added in small portions, transferred to a separatory funnel and the layers separated, followed by washing the aqueous layer with petroleum ether (2×50 mL). The combined petroleum ether extracts were washed with a 20% potassium carbonate solution, followed by a saturated sodium chloride solution and dried over magnesium sulfate. The combined organic layers were concentrated to give a yellow oil. Distillation of the residue yielded 3-chloro-but-2-enoic acid ethyl ester (7.4 g 43%) as a clear oil: LR-ES-MS m/z calculated for C6H9ClO2 [M]+ 148, observed [M+H]+ 149.