Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294522Generated: October 30, 2026

Triphenylphosphine → (3-Chlorophenylethynyl)trimethylsilane

https://huagongshe.com/reaction/1294522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-Chloro-3-iodobenzeneHCID 12269—
ReactantTrimethylsilylacetyleneHCID 66111—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product(3-Chlorophenylethynyl)trimethylsilaneHCID 411666659%

Reaction Steps

Chloro-3-iodobenzene (10.0 g, 41.9 mmol) was dissolved in 100 mL dry THF and 17.5 mL triethyl amine. This mixture was evacuated and backfilled with argon several times to remove oxygen from the solution. Triphenylphosphine (329 mg, 1.25 mmol) and bis(triphenylphosphine)palladium(II)chloride (1.47 g, 2.09 mmol) were added and the reaction mixture was stirred at room temperature for 1 h. Copper(I)iodide (239 mg, 1.25 mmol) and trimethylsilylacetylen (6.28 g, 6.39 mmol) were added. The reaction mixture was stirred at room temperature overnight. The solvent was evaporated. The residue was taken up in 500 mL water and extracted three times with ethyl acetate (500 mL each). The combined organic extracts were dried with magnesium sulfate, filtered and evaporated. The crude product was purified by flash-chromatography on silica gel (heptane/ethyl acetate 100:0->80:20 gradient). The desired product was obtained as a light yellow oil (7.38 g, purity ˜70%, yield ˜59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241760B2
Source datasetuspto-grants-2007_07
ORD IDord-dc3c51ad74ee4933b2a0e2f3352beb2b
Source noteuspto-grants-2007_07