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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380249Generated: October 30, 2026

Hydrochloric Acid → 4-(4-Fluorobenzoyl)pyridine

https://huagongshe.com/reaction/1380249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFluorobenzeneHCID 10008—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantIsonicotinoyl chloride hydrochlorideHCID 12262826—
Product4-(4-Fluorobenzoyl)pyridineHCID 702301975.5%

Reaction Steps

To a stirred and cooled (ice-bath) solution of 141.5 parts of 4-pyridinecarbonyl chloride hydrochloride in 400 parts of fluorobenzene were added portionwise 399 parts of aluminum chloride. Upon completion, the whole was slowly heated to reflux and stirring at reflux was continued for 6 hours. The reaction mixture is cooled, poured onto crushed ice and acidified with 240 parts of a hydrochloric acid solution 10N. The layers were separated. The acid aqueous phase was washed twice with 180 parts of methylbenzene and strongly alkalized with a sodium hydroxide solution 60%. The product was extracted three times with dichloromethane. The combined extracts were dried, filtered and evaporated. The residue was dissolved in 900 parts of methylbenzene and the solution was treated with activated charcoal. The latter was filtered off and the filtrate was evaporated. The residue was crystallized from 2,2'-oxybispropane, yielding 152 parts (75.5%) of (4-fluorophenyl)(4-pyridinyl)methanone; mp. 85.5° C. (intermediate 25).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581171
Source datasetuspto-grants-1986_04
ORD IDord-b8c3c49dbf0f4c3d9c3e82d55c8e2b9c
Source noteuspto-grants-1986_04