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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399361Generated: October 31, 2026

Trimethylsilylacetylene → HCID 178444321, compound

https://huagongshe.com/reaction/399361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 178444243HCID 178444243—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDiisopropylamineHCID 7912—
ProductHCID 178444321HCID 17844432169.3%

Reaction Steps

10.00 g (32.36 mmol) of 1-bromo-4-(trans-4-pentylcyclohexyl)benzene, 3.89 g (35.60 mmol) of trimethylsilylacetylene, 0.45 g (0.65 mmol) of bis(triphenylphosphine)palladium(II) chloride and 0.062 g (0.32 mmol) of copper(I) iodide are heated for 6 hours at the reflux temperature in 100 ml of diisopropylamine. The solvent is subsequently stripped off, and the soluble constituents of the residue are chromatographed on silica gel using n-hexane, giving 7.32 g of 1-(trimethylsilylethynyl)-4-(trans-4-pentylcyclohexyl)benzene, ##STR5## which is stirred for 1 hour at room temperature in 220 ml of methanol with 1.38 g (24.70 mmol) of potassium hydroxide. Work-up by evaporation of the solvent, partitioning between ether and water, drying and evaporation of the organic phase gives 4.95 g of 1-ethynyl-4-(trans-4-pentylcyclohexyl)benzene. ##STR6##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05820785
Source datasetuspto-grants-1998_10
ORD IDord-41ca4b025a0f4d35a51c7baa48dab03b
Source noteuspto-grants-1998_10