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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1885660Erstellt: 27. Oktober 2026

Hydrochloric Acid → 1,3-Bis(4-fluorobenzoyl)benzene

https://huagongshe.com/reaction/1885660

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktIsophthaloyl chlorideHCID 7451—
EduktFluorobenzeneHCID 10008—
EduktAluminum(III) ChlorideHCID 6451240—
Produkt1,3-Bis(4-fluorobenzoyl)benzeneHCID 68826381%

Reaktionsschritte

Anhydrous aluminum chloride (160.0 g, 1.20 mol) was added to a stirred solution of isophthaloyl chloride (101.5 g, 0.50 mol) dissolved in fluorobenzene (480.5 g, 5.0 mol) over a five to ten minute period. The mixture was stirred at room temperature for one hour and then maintained at 70°-80° C. for four hours. After cooling, the reaction mixture was poured onto approximately 2000 g of ice containing 100 mL of concentrated hydrochloric acid. The resulting suspension was separated by decantation and washed several times with water. The organic layer was distilled to remove excess fluorobenzene and the solid residue was collected by filtration, washed with water, and dried at 100° C. The crude solid was recrystallized from approximately 1000 mL of toluene to afford 130.5 g (81% yield) of 1,3-bis(4-fluorobenzoyl)benzene; m.p. 177.5°-178.5° C.; 1H NMR (CDCl3) δ 6.8-8.3 (m, 12H, aromatic). Anal. Calcd. for C20H12F2O2 : C, 74.53%; H, 3.75%; F, 11.79%. Found: C, 74.33%; H, 3.59%; F, 11.42%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05145942
Quelldatensatzuspto-grants-1992_09
ORD IDord-bf9ed53aebce45c4bbc1fbd113e2f42e
Quellennotizuspto-grants-1992_09