Sc. Shim et al., CARBONYLATION OF 1-BROMO-2,6-BIS(BROMOMETHYL)BENZENE CATALYZED BY COBALT CARBONYL, Bulletin of the Korean Chemical Society, 14(4), 1993, pp. 481-485
Dialkyl 1-bromobenzene-2,6-diacetates were easily prepared by the carb
onylation of the moiety of benzylic bromide in 1-bromo-2,6-bis(bromome
thyl)benzene with alcohol in the presence of NaOAc.3H2O and a catalyti
c amount of Co2 (CO)8 under the atmospheric pressure of carbon monoxid
e at room temperature in excellent yield. Alkyl 2,6-bis(alkoxymethyl)b
enzoates were obtained by the carbonylation of the moiety of aryl brom
ide in 1-bromo-2,6-bis(alkoxymethyl)-benzene, which derived from 1-bro
mo-2,6-bis(bromomethyl)benzene1, alcohol, NaOR, and CH3I under the sam
e conditions. Alkyl 2,6-bis(carboxymethyl)benzoate was also obtained i
n a trace amount for 24 hrs at room temperature.