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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190126Generated: November 1, 2026

Ethyl 5-bromo-4-(3-chlorophenyl)furan-2-carboxylate → 5-Bromo-4-(3-chlorophenyl)furan-2-carboxylic acid

https://huagongshe.com/reaction/2190126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-bromo-4-(3-chlorophenyl)furan-2-carboxylateHCID 58064768—
Reactant4-(3-Chloro-5-fluorophenyl)-5-(3-cyanophenyl)furan-2-carboxylic acidHCID 58064798—
Product5-Bromo-4-(3-chlorophenyl)furan-2-carboxylic acidHCID 58064802—

Reaction Steps

The preparation of the title compound takes place in analogy to the synthesis of the compound from Example 20A starting with the compound from Example 18A. The crude product obtained after extraction is dried under high vacuum and reacted further without chromatographic purification. 47.0 mg (86% of theory) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324268B2
Source datasetuspto-grants-2012_12
ORD IDord-d95bb25cf0934d10b758a3700952141b
Source noteuspto-grants-2012_12