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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885657Generated: October 30, 2026

Hydrochloric Acid → [4-(4-Fluorobenzoyl)phenyl]-(4-fluorophenyl)methanone

https://huagongshe.com/reaction/1885657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTerephthaloyl chlorideHCID 7488—
ReactantFluorobenzeneHCID 10008—
ReactantAluminum(III) ChlorideHCID 6451240—
Product[4-(4-Fluorobenzoyl)phenyl]-(4-fluorophenyl)methanoneHCID 1114180488%

Reaction Steps

Anhydrous aluminum chloride (80.0 g, 0.60 mol) was added to a stirred solution of terephthaloyl chloride (50.8 g, 0.25 mol) dissolved in fluorobenzene (235 ml, 2.5 mol) over a 10-15 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 1000 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 collected by filtration, washed with water, and dried at 100° C. The crude solid was recrystallized from approximately 2000 ml of toluene to afford 70.7 g (88% yield) of 1,4-bis(4-fluorobenzoyl)-benzene; mp 218.5°-219.5° C.; Anal. Calcd for C20H12F2O2 : C, 74.53%; H, 3.75%; F, 11.179%. Found: C, 74.60%; H, 3.80%; F, 11.83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05145937
Source datasetuspto-grants-1992_09
ORD IDord-0896f7a069114cef8c71882a43293ed7
Source noteuspto-grants-1992_09