Reacción #1265350

ord-94c136a4de24494fa3bf6dc0df23b1cc

Ecuación de reacción

O=C(Cl)C(=O)Cl
Oxalyl chloride
COCCOCCOCC(=O)O
2-[2-(2-methoxy-ethoxy)ethoxy]-acetic acid
c1ccncc1
pyridine
COCCOCCCOCC(=O)Cl
CH3(OCH2CH2)2CH2OCH2COCl

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónThe reaction solution was concentrated in vacuo

Procedimiento

Oxalyl chloride (100 g, 0.78 mol) was added dropwise over 1 h to a solution of 2-[2-(2-methoxy-ethoxy)ethoxy]-acetic acid (90 mL, 0.59 mol) and pyridine (0.1 mL, 1 mmol) in anhydrous toluene (250 mL) and the resulting solution was stirred at ambient temperature for 48 h. The reaction solution was concentrated in vacuo to afford CH3(OCH2CH2)2CH2OCH2COCl as a slightly yellow oil (120 g, 96%). This compound was used without any further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07276286B2uspto-grants-2007_10