Reacción #367212
ord-b37f6d563f0f43dea23f939cc7c3bba2
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturawas heated
- 2Temperaturaat reflux for 24 hr
- 3Temperaturato cool
- 4ExtracciónThe resultant mixture was extracted with toluene (1×200 mL and 2×100 mL)
- 5ExtracciónThe combined toluene portions were extracted with water (3×100 mL)
- 6Secadodried over magnesium sulfate
- 7ConcentraciónThe toluene solution was concentrated
- 8Otroleaving a brown oil which
- 9workup.DISTILLATIONwas distilled under reduced pressure
Procedimiento
A mixture of sodium methoxide (8.86 g, 0.164 mole), and 3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)-2-methoxymethylpropenenitrile (Example 37A, 23.1 g, 0.080 mole) in methanol (60 mL) was heated at reflux for 24 hr, allowed to cool and diluted with water (200 mL). The resultant mixture was extracted with toluene (1×200 mL and 2×100 mL). The combined toluene portions were extracted with water (3×100 mL) and dried over magnesium sulfate. The toluene solution was concentrated leaving a brown oil which was distilled under reduced pressure to give 15.9 g (62%) of a yellow oil which was used without further purification.