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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650360Generated: October 31, 2026

Boron trifluoride → [4-(4-Fluorobenzoyl)phenyl]-(4-fluorophenyl)methanone

https://huagongshe.com/reaction/1650360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
ReactantTerephthaloyl chlorideHCID 7488—
ReactantFluorobenzeneHCID 10008—
ReactantHydrofluoric AcidHCID 14917—
Product[4-(4-Fluorobenzoyl)phenyl]-(4-fluorophenyl)methanoneHCID 11141804122.6%

Reaction Steps

20.3 g of terephthaloyl dichloride, 19.2 g of fluorobenzene and 50 g of hydrogen fluoride were initially introduced into a 250 ml stainless steel autoclave and boron trifluoride was introduced under pressure at 10 bar. The autoclave was shaken for 16.5 h at room temperature. Working-up was carried out by initially evaporating the volatile components at room temperature and then at 60° to 100° C. and recrystallizing the residue from chlorobenzene in the presence of sodium carbonate. 19.76 g of 1,4-bis-(4-fluorobenzoyl)-benzene were obtained in the form of colorless crystals of m.p. 221° C. Examination by means of high pressure liquid chromatography (HPLC) gave a degree of purity of 99.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04924014
Source datasetuspto-grants-1990_05
ORD IDord-02cb75b589704f51b7d314d24a3b86e8
Source noteuspto-grants-1990_05