Reacción #58476
ord-c127cb7733094ef09bbaf4730a2d36ae
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Extracciónextracted with CH2Cl2 (4×30 ml)
- 2SecadoThe organic layers were dried over sodium sulfate
- 3Concentraciónconcentrated
Procedimiento
To a solution of 4-oxotetrahydro thiophene-3-carboxylic acid methyl ester (4 g, 25 mmol) in methanol (7 ml), cooled at 0° C., a solution of potassium cyanide (1.68 g, 30 mmol) in water (10 ml) was added. The mixture was acidified with acetic acid (1.5 ml, 25 mmol) and stirred at 0° C. for 8 hours. Then the mixture was acidified with H3PO4 and diluted with brine (50 ml) and extracted with CH2Cl2 (4×30 ml). The organic layers were dried over sodium sulfate and concentrated to give 4-cyano-tetrahydro thiophene-3-carboxylic acid methyl ester in 75% yield.