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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549818Generated: October 31, 2026

4-Bromobenzophenone → phenyl-[4-(phenylethynyl)phenyl]methanone

https://huagongshe.com/reaction/549818

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzophenoneHCID 7030—
ReactantDiisopropylamineHCID 7912—
ReactantCyclohexaneHCID 8078—
ReactantPhenylacetyleneHCID 10821—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
Productphenyl-[4-(phenylethynyl)phenyl]methanoneHCID 2179865—

Reaction Steps

In argon atmosphere, 0.15 M Solution of tri-tert-butylphosphine in cyclohexane (12.0 mL, 18.0 mmol) was added to a stirred suspension of copper(I) iodide (350 mg, 1.8 mmol) and dichloro(bisbenzonitrile)palladium (350 mg, 0.9 mmol) in tetrahydrofuran (100 mL) at ambient temperature. The mixture was stirred for 5 min, N,N-diisopropylamine (4.5 mL, 30 mmol) was added, the mixture was stirred for next 5 min and then a solution of 4-bromobenzophenone (3.92 g, 15 mmol) and phenylacetylene (2.30 g, 22.5 mmol) in tetrahydrofuran (20 mL) was added dropwise during 15 min. The reaction mixture was stirred at ambient temperature overnight and then diluted with benzene (200 mL). The benzene solution was washed with water (2×80 mL) and 1.5 M aqueous solution of tartaric acid (30 mL); the organic solution was dried with anhydrous magnesium sulfate and subsequently evaporated in vacuo. The residue was purified by column chromatography (silica gel Fluka 60, hexane/ethyl acetate 95:5) yielding phenyl-[4-(phenylethynyl)phenyl]methanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943613B2
Source datasetuspto-grants-2011_05
ORD IDord-c9be3e665a5849079b3825c9a1821652
Source noteuspto-grants-2011_05