Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372314Generated: October 31, 2026

Ethyl bromoacetate → 1-Ethoxycarbonyl-5-chloro-3-phenylisoindole-2-acetic acid ethyl ester

https://huagongshe.com/reaction/372314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantEthyl 5-chloro-3-phenyl-2H-isoindole-1-carboxylateHCID 54174784—
SolventDimethyl SulfoxideHCID 679—
Product1-Ethoxycarbonyl-5-chloro-3-phenylisoindole-2-acetic acid ethyl esterHCID 54561252—

Reaction Steps

A solution of 30.0 g. of 5-chloro-3-phenyisoindole-1carboxylic acid ethyl ester in 300 ml. of dimethylsulfoxide is treated with 66.8 g. of bromoacetic acid ethyl ester and 27.6 g. of finely triturated, dry potassium carbonate and intensively stirred at room temperature for 17 hours. The mixture is poured into 750 ml. of ice-water and the separated product, after the addition of 50 g. of sodium chloride, is removed by filtration under suction, washed with water and then dissolved in methylene chloride. The aqueous layer is separated, the organic phase dried over sodium sulfate, filtered and concentrated to dryness. The resulting oil crystallizes on trituration with ether and pentane, and there is obtained 1-ethoxycarbonyl-5-chloro-3-phenylisoindole-2-acetic acid ethyl ester; melting point 100°-101° C. Recrystallization from ethanol increases the melting point to 103°-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04090027
Source datasetuspto-grants-1978_05
ORD IDord-abc48127678e460c95fa5dd24564e751
Source noteuspto-grants-1978_05