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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190118Generated: November 1, 2026

Ethyl 4-bromo-5-(3-chloro-4-fluorophenyl)furan-2-carboxylate → Ethyl 5-(3-chloro-4-fluorophenyl)-4-(3-chloro-5-fluorophenyl)furan-2-carboxylate

https://huagongshe.com/reaction/2190118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-bromo-5-(3-chloro-4-fluorophenyl)furan-2-carboxylateHCID 58064794—
ReactantEthyl 4-(3-chloro-5-fluorophenyl)-5-(3-cyanophenyl)furan-2-carboxylateHCID 58064795—
ProductEthyl 5-(3-chloro-4-fluorophenyl)-4-(3-chloro-5-fluorophenyl)furan-2-carboxylateHCID 58064790—

Reaction Steps

The preparation of the title compound takes place in analogy to the synthesis of the compound from Example 11A starting with the compound from Example 6A. Purification is carried out using the mobile phase: cyclohexane/ethyl acetate (50:1). 1.07 g (63% of theory) of the title compound with a purity of 81% are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324268B2
Source datasetuspto-grants-2012_12
ORD IDord-0d7189686283479f9b9202a8373168ee
Source noteuspto-grants-2012_12