Reacción #984

ord-6120ae4e516c4335a3f2eb3671f18da1

Ecuación de reacción

COC(=O)c1ccc(C=O)cc1
aldehyde
COC(=O)c1ccc(C=O)cc1
4-Formylbenzoic acid methyl ester
CC(C1OCCCO1)[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]
[1-(1,3-dioxan-2-yl)ethyl]triphenylphosphoniumbromide
[Li][CH2]CCC
n-BuLi
COC(=O)c1ccc(C=CCC2OCCO2)cc1
olefin
Rendimiento 50.3%
COC(=O)c1ccc(C=CCC2OCCO2)cc1
4-[3-[1,3]-Dioxolan-2-yl -propenyl)benzoic acid methyl ester
Rendimiento 50.3%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    LavadoFlash chromatography (elution with 10% ethyl acetate in hexane)

Procedimiento

The olefin was prepared from 4.3 g (26.2 mmol) of the aldehyde 167, 13.94 g of [1-(1,3-dioxan-2-yl)ethyl]triphenylphosphoniumbromide and 12.6 mL (32.0 mmol) of n-BuLi in 75 mL of THF as described for the synthesis of 156 in Example 8. Flash chromatography (elution with 10% ethyl acetate in hexane) gave 3.27 g of the olefin 168. 1H NMR consistent with the product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723459uspto-grants-1998_03