Reacción #575316
ord-4e68f7a3e46c4e7e9c03fad0d13a0691
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otroirradiated with light from a high pressure mercury lamp through a Pyrex
- 2Filtraciónfilter at room temperature for 3 hours
- 3ConcentraciónThe reaction mixture was concentrated in vacuo
- 4Otropurified by silica gel column chromatography (3% methanol/chloroform)
Procedimiento
1.15 g of (E)-3-(4-acetoxy-5-ethyl-3-methoxy-1-naphthyl)-2-methylpropenoic acid was dissolved in 200 ml of acetone and irradiated with light from a high pressure mercury lamp through a Pyrex filter at room temperature for 3 hours. The reaction mixture was concentrated in vacuo and purified by silica gel column chromatography (3% methanol/chloroform) to obtain 470 mg of the titled compound as colorless crystals.