Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51741Generated: October 26, 2026

Methyl 4-Iodophenylacetate → Methyl{4-[4-(1-benzyloxycyclopropyl)-3-ethyl-phenylethynyl]-phenyl}-acetate

https://huagongshe.com/reaction/51741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-IodophenylacetateHCID 10378700—
Reactant1-Ethynyl-4-(1-benzyloxycyclopropyl)-3-ethyl-benzeneHCID 22568983—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductMethyl{4-[4-(1-benzyloxycyclopropyl)-3-ethyl-phenylethynyl]-phenyl}-acetateHCID 8658592779%

Reaction Steps

Using General Procedure F; 1-ethynyl-4-(1-benzyloxycyclopropyl)-3-ethyl-benzene (Intermediate 90, 107.0 mg, 0.39 mmol) and methyl-(4-iodophenyl)-acetate (Reagent B, 110.0 mg, 0.39 mmol) in triethylamine (5 mL) was treated with copper(I)iodide (25.0 mg, 0.13 mmol) and sparged with argon for 5 minutes. Dichlorobis(triphenylphosphine)palladium(II) (91 mg, 0.13 mmol) was added and the reaction mixture was stirred overnight at room temperature. Column chromatography (2-4% EtOAc-hexanes) afforded 130.0 mg (79%) of the title compound as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713647B2
Source datasetuspto-grants-2004_03
ORD IDord-9df2df3a27b747bab5c4878d97999326
Source noteuspto-grants-2004_03