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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472500Generated: October 29, 2026

Tetrahydrofuran → Methyl 4-chloro-3-(2-(4-fluorophenyl)ethynyl)benzoate

https://huagongshe.com/reaction/1472500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-Ethynyl-4-fluorobenzeneHCID 522627—
ReactantMethyl 4-chloro-3-iodobenzoateHCID 15521790—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductMethyl 4-chloro-3-(2-(4-fluorophenyl)ethynyl)benzoateHCID 70654480—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under an inert atmosphere of nitrogen, a mixture of methyl 4-chloro-3-iodobenzoate (200 mg, 0.68 mmol, 1.00 equiv), 1-ethynyl-4-fluorobenzene (243 mg, 2.02 mmol, 3.00 equiv), Pd(PPh3)2Cl2 (94.6 mg, 0.14 mmol, 0.20 equiv), CuI (13 mg, 0.07 mmol, 0.10 equiv), tetrahydrofuran (12 mL), and triethylamine (4 mL) was stirred overnight at 70° C. in an oil bath. The solids were filtered out, and the filtrate was concentrated in vacuo. The residue was purified via silica gel column chromatography (ethyl acetate/petroleum ether (1:100)) resulting in 130 mg (67%) of methyl 4-chloro-3-(2-(4-fluorophenyl)ethynyl)benzoate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012637B2
Source datasetuspto-grants-2015_04
ORD IDord-f908cedb16ff46909627573389de1d69
Source noteuspto-grants-2015_04