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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 462678Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/462678

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBenzoyl chlorideHCID 7412—
Edukt4-Fluoro-1,2-dimethoxybenzeneHCID 593640—
EduktAluminum(III) ChlorideHCID 6451240—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt(4,5-Dimethoxy-2-fluorophenyl)-phenylmethanoneHCID 20396992—

Reaktionsschritte

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°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04517184
Quelldatensatzuspto-grants-1985_05
ORD IDord-fa2ad09f21464bcea9712e88cf0cccf0
Quellennotizuspto-grants-1985_05