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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24239Generated: October 28, 2026

Methyl 4-Iodophenylacetate → Methyl[4-(4-imidazol-1-yl-methyl-3-methyl-phenylethynyl)-phenyl]-acetate

https://huagongshe.com/reaction/24239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-IodophenylacetateHCID 10378700—
ReactantEthylacetate methanolHCID 21584119—
ReactantHCID 22568804HCID 22568804—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductMethyl[4-(4-imidazol-1-yl-methyl-3-methyl-phenylethynyl)-phenyl]-acetateHCID 8658593125%

Reaction Steps

Using General Procedure F; 1-(4-ethynyl-2-methyl-benzyl)-1H-imidazole (Intermediate 141, 101.0 mg, 0.53 mmol) and methyl-(4-iodophenyl)-acetate (Reagent B, 145.0 mg, 0.53 mmol) in triethylamine (5 mL) was treated with copper(I)iodide (34.0 mg, 0.18 mmol) and sparged with argon for 5 minutes. Dichlorobis(triphenylphosphine)palladium(II) (124 mg, 0.18 mmol) was added and the reaction mixture was stirred overnight at room temperature. Column chromatography (5% MeOH-EtOAc) afforded 45.0 mg (25%) of the title compound as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855512B2
Source datasetuspto-grants-2005_02
ORD IDord-09fd58ca65134ee0a77f2816da9a9f38
Source noteuspto-grants-2005_02