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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369558Generated: October 24, 2026

Hydrochloric Acid → 4-Fluoro-4'-(phenylethynyl)benzophenone

https://huagongshe.com/en/reaction/369558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenylacetyleneHCID 10821—
ReactantTriphenylphosphineHCID 11776—
Reactant(4-Bromophenyl)(4-fluorophenyl)methanoneHCID 74951—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
Product4-Fluoro-4'-(phenylethynyl)benzophenoneHCID 4095657—

Reaction Conditions

Temperature23 °C

Reaction Steps

4-Fluoro-4'-phenylethynylbenzophenone was synthesized by the cuprous iodide catalyzed coupling of 4-bromo-4'-fluorobenzophenone. More specifically, 4-bromo-4'-fluorobenzophenone (30 grams, 0.11 mol), phenylacetylene (11 grams, 0.11 mol), triphenylphosphine (0.2 gram), cuprous iodide (0.1 gram), bis(triphenylphosphine) palladium dichloride (0.1 gram) and 450 milliliters of triethylamine were charged to a 500 milliliter flask equipped with a mechanical stirrer, N2 inlet, and reflux condenser. The mixture was heated to reflux for 4 hours, cooled to 23° C., and stirred for an additional 16 hours. The mixture was then poured into water acidified with HCl and the precipitate was collected by filtration. Recrystallization from acetone gave 23 grams (75 percent yield) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06139920
Source datasetuspto-grants-2000_10
ORD IDord-c4709ef325e24f80b7a8bb3c436bd115
Source noteuspto-grants-2000_10