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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648709Generated: October 26, 2026

Benzene → 3-Benzoyl-2-chloropyridine

https://huagongshe.com/reaction/648709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantWaterHCID 962—
Reactant2-Chloronicotinoyl chlorideHCID 2774541—
ReactantAluminum(III) ChlorideHCID 6451240—
Product3-Benzoyl-2-chloropyridineHCID 824619—

Reaction Steps

To a cooled solution of 150 g 2-chloro-nicotinoyl chloride in 400 ml benzene there is added slowly 238 g AlCl3. After refluxing 2 hrs. the reaction mixture is added with stirring to a slightly acidic ice: water mixture. The organic layer is separated and the aqueous one is extracted with ethyl ether. The combined organic layers are washed with HONa 1N, then with water, and dried over Na2SO4. The excess benzene is distilled at water pump pressure in a rotary evaporator and the residual oil is distilled in vacuo. Yield: 157 g of title product, b.p. 123° C./0.05 mm; m.p. 35°-7° C.; UV (ethanol): λmax. 254 nm., ε: 17,180; Cl 15.97 (16.29).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04736037
Source datasetuspto-grants-1988_04
ORD IDord-ef3affb0918342708ced581bb98ca27d
Source noteuspto-grants-1988_04