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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462678Generated: October 26, 2026

Hydrochloric Acid → (4,5-Dimethoxy-2-fluorophenyl)-phenylmethanone

https://huagongshe.com/reaction/462678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzoyl chlorideHCID 7412—
Reactant4-Fluoro-1,2-dimethoxybenzeneHCID 593640—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
Product(4,5-Dimethoxy-2-fluorophenyl)-phenylmethanoneHCID 20396992—

Reaction Steps

12.7 g (95 mmol) of aluminium trichloride in 80 ml of 1,2-dichloroethane are stirred under nitrogen and cooled to 3°. 13.35 g (95 mmol) of benzoyl chloride are added. At 30°, this red solution is added dropwise over a period of 25 minutes to a solution of 12.55 g (80.3 mmol) of 1,2-dimethoxy-4-fluorobenzene (4-fluoroveratrole) in 80 ml of 1,2-dichloroethane. The reaction mixture is stirred for a further 3 hours at 3°, then for 31/2 hours at room temperature and then poured onto a mixture of 250 ml of ice and 20 ml of concentrated hydrochloric acid. The organic phase is separated off and the aqueous phase is extracted several times with ether. Organic phase and ether solutions are combined, washed with 1N sodium hydroxide solution, water and with saturated sodium chloride solution, dried over magnesium sulphate and concentrated by evaporation. The resulting yellow oil is stirred with 50 ml of ether in an ice bath until crystallisation takes place, yielding the desired (4,5-dimethoxy-2-fluorophenyl)-phenylmethanone in the form of white crystals having a melting point of 102°-103°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04517184
Source datasetuspto-grants-1985_05
ORD IDord-fa2ad09f21464bcea9712e88cf0cccf0
Source noteuspto-grants-1985_05