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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071687Generated: November 1, 2026

HCID 21411844, compound → [4-Bromo-5-(4-chlorobenzoyl)-1-methyl-1H-pyrrol-2-yl]acetic acid

https://huagongshe.com/reaction/2071687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21411844HCID 21411844—
CatalystEthanolHCID 702—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product[4-Bromo-5-(4-chlorobenzoyl)-1-methyl-1H-pyrrol-2-yl]acetic acidHCID 21411835—

Reaction Steps

A suspension of 0.9 g. of ethyl 4-bromo-5-(p-chlorobenzoyl)-1-methylpyrrole-2-acetate in 5 ml of 0.5N sodium hydroxide solution containing a few drops of ethanol is heated under reflux for one hour. At the end of 1 hour it is cooled, diluted with water and filtered, and the filtrate washed with ether. The aqueous filtrate is then acidified with dilute hydrochloric acid and the resulting precipitated solid is collected and air dried. Recrystallization thereof from acetonitrile gives 4-bromo-5-(p-chlorobenzoyl)- 1-methylpyrrole-2-acetic acid as a pink solid; m.p. 190° C. (dec.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04048191
Source datasetuspto-grants-1977_09
ORD IDord-b44059f724d6403aba81c9e589b6ea72
Source noteuspto-grants-1977_09