Reacción #5449

ord-623055db120040d483ebba9a6496e49a

Ecuación de reacción

O
H2O
CC(C)(C)[O-].[K+]
Potassium t-butoxide
CCOC(=O)CCCc1cc(OC)ccc1Br
ethyl -4-(2-bromo-5-methoxy phenyl)butyrate
CCOC(=O)C(=O)OCC
diethyl oxalate
CCOC(=O)C(=O)C(CCc1cc(OC)ccc1Br)C(=O)OCC
desired product
Rendimiento 89.0%
CCOC(=O)C(=O)C(CCc1cc(OC)ccc1Br)C(=O)OCC
2-Oxo-3-carboethoxy-5-(2-bromo-5-methoxyphenyl)pentanoic acid ethyl ester
Rendimiento 89.0%

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe aqueous layer was separated
  2. 2
    Extracciónextracted with ether
  3. 3
    SecadoThe ether layer was dried (MgSO4)
  4. 4
    Otrothe solvent was evaporated

Procedimiento

Potassium t-butoxide (26.94 g) was suspended in 130 ml of anhydrous ether and cooled to 0° C. A solution of 60.24 g ethyl -4-(2-bromo-5-methoxy phenyl)butyrate and 43.84 g diethyl oxalate in 60 ml ether was added dropwise over 20 min. After 2 h at 25° C., the reaction was poured into 400 ml H2O and the aqueous layer was separated, acidified to pH 1 and extracted with ether. The ether layer was dried (MgSO4) and the solvent was evaporated to yield 71.26 g of the desired product as a colorless oil (89%). NMR (CDCl3) δ 1.25 (t, 3H), 1.4 (t, 3H), 2.25 (m, 2H), 2.75 (m, 2H), 3.78 (s, 3H), 4.0-4.5 (m, 5H), 6.64 (dd, 1H), 6.79 (d, 1H), 7.40 (d, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05244888uspto-grants-1993_09