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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642913Generated: October 27, 2026

Tetrahydrofuran → 1-bromo-4-(phenylethynyl)benzene

https://huagongshe.com/reaction/642913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPhenylacetyleneHCID 10821—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTriethylamineHCID 8471—
Product1-bromo-4-(phenylethynyl)benzeneHCID 29088858.3%

Reaction Steps

28.3 g (0.10 mol) of p-bromoiodobenzene, 10.2 g (0.10 mol) of phenylacetylene, 701 mg (1 mmol) of bis(triphenylphosphine)palladium(II)dichloride, and 190 mg (1 mmol) of copper (I) iodide were placed in a 1000-mL three-neck flask, and nitrogen substitution was carried out. Then, 350 mL of tetrahydrofuran and 18 mL of triethylamine were added thereto, and the mixture was stirred at room temperature for 12 hours. After the reaction, the reaction mixture washed with a 3% hydrochloric acid aqueous solution, and the aqueous phase was extracted with ethyl acetate. The extracted solution combined with the organic phase washed with brine and dried with magnesium sulfate. The mixture was filtered through celite, florisil, and alumina, and a solid obtained by the concentration of the filtrate was recrystallized with hexane to give 15 g of a solid that was the target substrate in the yield of 58%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696348B2
Source datasetuspto-grants-2010_04
ORD IDord-54a909303b374952a064f6f8bd93760e
Source noteuspto-grants-2010_04