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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701814Generated: November 2, 2026

Boron trifluoride → 2-Benzoylbenzoic Acid

https://huagongshe.com/reaction/1701814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
ReactantPhthalic AnhydrideHCID 6811—
SolventBenzeneHCID 241—
Product2-Benzoylbenzoic AcidHCID 6813177%

Reaction Conditions

Temperature20 °C

Reaction Steps

7.4 g of phthalic anhydride and 3.9 of benzene were charged at ambient temperature into a stainless steel autoclave. The autoclave was cooled by liquid nitrogen and 10 g of HF and 37.4 g of BF3 were introduced. The autoclave was heated to 20° C. and the pressure raised to 47 bars. The temperature was maintained at 20° C. for 15 minutes and the product degassed under reduced pressure in order to recover the catalyst. After washing with cold water, 10 g of crude o-benzoyl benzoic acid were obtained titrating 74.4% and containing 0.5% of anthraquinone, thus a chemical yield of 66%. After purification by extraction with 600 cm3 of boiling water, then crystallization by cooling to 20° C., o-benzoyl benzoic acid titrating 98.4% was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379092
Source datasetuspto-grants-1983_04
ORD IDord-9cc0ab097477443f810fc5244b17d3df
Source noteuspto-grants-1983_04