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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24160Generated: October 26, 2026

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

https://huagongshe.com/reaction/24160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-IodophenylacetateHCID 10378700—
ReactantMethyl{4-[4-(1-benzyloxycyclopropyl)-phenylethynyl]-phenyl}-acetateHCID 86585923—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductMethyl{4-[4-(1-benzyloxycyclopropyl)-3-methyl-phenylethynyl]-phenyl}-acetateHCID 8658592471%

Reaction Steps

Using General Procedure F; 1-ethynyl-4-(1-benzyloxycyclopropyl)-3-methyl-benzene (Intermediate 76, 90.0 mg, 0.34 mmol) and methyl-(4-iodophenyl)-acetate (Reagent B, 95.0 mg, 0.34 mmol) in triethylamine (5 mL) was treated with copper(I)iodide (22.0 mg, 0.11 mmol) and sparged with argon for 5 minutes. Dichlorobis(triphenylphosphine)palladium(II) (80 mg, 0.11 mmol) was added and the reaction mixture was stirred overnight at room temperature. Column chromatography (2-4% EtOAc—hexanes) afforded 90.0 mg (71%) of the title compound as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855512B2
Source datasetuspto-grants-2005_02
ORD IDord-197fe290f55f44e3ad8a89d368680513
Source noteuspto-grants-2005_02