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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085611Generated: October 26, 2026

Ethyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylate → 5-Bromo-4-(p-chlorophenyl)pyrrole-3-carboxylic acid

https://huagongshe.com/reaction/1085611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylateHCID 15010185—
SolventSodium HydroxideHCID 14798—
Product5-Bromo-4-(p-chlorophenyl)pyrrole-3-carboxylic acidHCID 15753018—

Reaction Steps

Ethyl 5-bromo-4-(p-chlorophenyl)pyrrole-3-carboxylate (15 g., 0.045 mmol) is added to 200 mL of 10% sodium hydroxide and the slurry heated to reflux. After everything appears to dissolve the mixture is refluxed an additional 40 minutes. The mixture is cooled, filtered and the filtrate acidified. The white precipitate (8.0 g, 58%) is collected and dried. The solid has m.p. >205° C. and an NMR (d6 -DMSO) which showed a pyrrole proton at 7.52 (d). The mass spectrum is also consistent for a monobrominated compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05010098
Source datasetuspto-grants-1991_04
ORD IDord-d04f56ed83d7470fb8982b7ad4ed849c
Source noteuspto-grants-1991_04