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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199594Generated: November 3, 2026

Triethylamine → (4-Chlorophenylethynyl)trimethylsilane

https://huagongshe.com/reaction/1199594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Chloro-4-iodobenzeneHCID 12510—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylsilylacetyleneHCID 66111—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventHexaneHCID 8058—
Product(4-Chlorophenylethynyl)trimethylsilaneHCID 333729893.4%

Reaction Steps

To a solution of 4-chloroiodobenzene (4.77 g:0.02 mole) in dry acetonitrile (30 ml) and triethylamine (2.02 g:0.02 mole) under nitrogen, was added copper iodide (0.2 g:1.05 mole), bis (triphenylphosphine)palladium dichloride (0.2 g=0.285 mmole) and trimethylsilylethyne (2.156 g:0.022 mole). The mixture was stirred for three hours during which time there was an exotherm at 20° C. and a darkening of the reacton mixture. The mixture was poured into saturated ammonium chloride solution (100 ml) and was extracted with ether (×3). The extracts were combined, washed with dilute hydrochloric acid and dried over magnesium sulfate and then filtered through charcoal. Removal of solvent in vacuo gave a brown oil which was titurated with hexane and filtered to remove by-products. The filtrate was evaporated to give yellow crystals (3.90 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04902332
Source datasetuspto-grants-1990_02
ORD IDord-ea74fe9d39b449a4ac066e630643b61a
Source noteuspto-grants-1990_02