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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991867Generated: October 31, 2026

Ethyl 4-ethynylbenzoate → HCID 56987556, compound

https://huagongshe.com/reaction/991867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-ethynylbenzoateHCID 15540683—
ReactantHCID 57287130HCID 57287130—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTriethylamineHCID 8471—
ProductHCID 56987556HCID 56987556—

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of 2-(2-methyl-6-oxocyclohex-1-enyl)-1-iodoethene (Compound E, 1.74 g, 6.64 mmol), ethyl 4-ethynylbenzoate (Compound F, 1.73 g, 9.96 mmol) and triethylamine (80 mL) was purged with argon for 10 minutes, and then treated with bis(triphenylphosphine)palladium (II) chloride (23 mg, 0.03 mmol) and copper (I) iodide (6.3 mg, 0.03 mmol). The solution was stirred 40° C. for 3 hours, and concentrated under a water aspirator vacuum. The residue was dissolved in ethyl acetate and washed with saturated aqueous NH4Cl. The layers were separated and the aqueous layer was extracted twice with ethyl acetate. The combined organic fractions were washed with water, and brine, and dried (MgSO4). The solvents were removed under reduced pressure, and the residue was purified by silica gel chromatography (88:12, hexane:ethyl acetate) to give the title compound as a yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465646B1
Source datasetuspto-grants-2002_10
ORD IDord-56b4cec64d2c4d2182af51124aa9d53b
Source noteuspto-grants-2002_10