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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707880Generated: November 2, 2026

Trimethylsilylacetylene → HCID 15745229, compound

https://huagongshe.com/reaction/1707880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 18960147HCID 18960147—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDiethylamineHCID 8021—
ProductHCID 15745229HCID 15745229—

Reaction Steps

A mixture of 0.1 mol of 4-pentyl-2-fluoro-iodobenzene, 0.12 mol of trimethylsilylacetylene, 0.0014 mol of bis(triphenylphosphine)-palladium(II) chloride Pd(PPh3)2Cl2 and 0.7 mmol of copper (I) iodide in 250 ml diethylamine is stirred at room temperature for 20 hours. After evaporation of the solvent the crude product is purified by chromatography on alumina (4:1 petrol/difluoromethane) to give 2-(4-pentylphenyl)-1-trimethylsilylacetylene. Removal of the trimethylsilylgroup is accomplished by treatment this acetylene in methanol with 1M KOH for 1 hour at room temperature. Evaporation of the methanol and either extraction yields 4-pentyl-2-fluoro-phenylacetylene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356562
Source datasetuspto-grants-1994_10
ORD IDord-3dad28e912744b6488ddce920835fd16
Source noteuspto-grants-1994_10