Reacción #575316

ord-4e68f7a3e46c4e7e9c03fad0d13a0691

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroirradiated with light from a high pressure mercury lamp through a Pyrex
  2. 2
    Filtraciónfilter at room temperature for 3 hours
  3. 3
    ConcentraciónThe reaction mixture was concentrated in vacuo
  4. 4
    Otropurified 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05298649uspto-grants-1994_03