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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450852Generated: October 25, 2026

4-Chloropyridine → 5-Chloro-2-(2-morpholinobenzoyl)-benzofuran

https://huagongshe.com/reaction/450852

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChloropyridineHCID 12288—
ReactantEthyl 5-chlorobenzofuran-2-carboxylateHCID 2799299—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-2-(2-morpholinobenzoyl)-benzofuranHCID 69284462—

Reaction Steps

A solution of ethyl 5-chlorobenzofuran-2-carboxylate (350 mg, 1.56 mmol) in THF (10 ml) is added at −70° C. to a THF solution of lithiated 4-chloropyridine (1.8 mmol prepared according to G. Quéguiner et al., Synthesis 1986, 886-891). The mixture is allowed to reach room temperature within 16 hours before quenching with acetic acid. The product is extracted with chloroform. Drying and chromatography on silicagel gives the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486996B2
Source datasetuspto-grants-2013_07
ORD IDord-87f9061cd16240e8b1cc4d37ba8988e8
Source noteuspto-grants-2013_07