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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368968Generated: October 30, 2026

Hydrochloric Acid → 2-Chloro-3-(3-chlorobenzoyl)-6-ethylpyridine

https://huagongshe.com/reaction/368968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Bromo-3-chlorobenzeneHCID 7928—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant2-Chloro-6-ethylnicotinonitrileHCID 21930433—
Product2-Chloro-3-(3-chlorobenzoyl)-6-ethylpyridineHCID 2328448922%

Reaction Steps

Magnesium (2.72 g, 112 mmol) was added to a tetrahydrofuran (200 ml) solution of 3-bromochlorobenzene (22.1 g, 115 mmol), and the mixture was stirred at room temperature. Since spontaneous exothermic reaction occurred, the stirring was continued until the exothermicity was ceased. The reaction solution was cooled to -20° C., mixed with 2-chloro-3-cyano-6-ethylpyridine (9.33 g, 56 mmol) and then stirred for 16 hours at room temperature. The reaction solution was mixed with saturated ammonium chloride aqueous solution and stirred for 30 minutes at room temperature and then mixed with 1 N hydrochloric acid and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, magnesium-sulfate was removed by filtration and then the filtrate was concentrated under a reduced pressure. Thereafter, the resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give 2-chloro-3-(3-chlorobenzoyl)-6-ethylpyridine (3.48 g, 22%) as a pale yellow oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136810
Source datasetuspto-grants-2000_10
ORD IDord-dde86781619949e4b9cc33ec682b99d2
Source noteuspto-grants-2000_10