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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991864Generated: October 31, 2026

HCID 11299597, compound → HCID 57027195, compound

https://huagongshe.com/reaction/991864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11299597HCID 11299597—
ReactantHCID 57287130HCID 57287130—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTriethylamineHCID 8471—
ProductHCID 57027195HCID 57027195—

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of 1-iodo-2-(2-methyl-6-oxocyclohex-1-enyl)ethene (Compound E, available in accordance with the teachings of U.S. Pat. No. 5,760,276, 0.70 g, 2.67 mmol), (trimethylsilyl)ethyl 4-ethynylbenzoate (Compound C, 0.79 g, 3.21 mmol) and triethylamine (32 ml) was purged with argon for 10 minutes, and then treated with bis(triphenylphosphine)palladium (II) chloride (47 mg, 0.07 mmol) and copper (I) iodide (12.8 mg, 0.07 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 (90:10, hexane:ethyl acetate) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465646B1
Source datasetuspto-grants-2002_10
ORD IDord-8b7e5ba01d2c45b683cbfd619b8d77b9
Source noteuspto-grants-2002_10