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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673394Generated: October 31, 2026

Hydrochloric Acid → Methyl 2-(benzamido)-4-(phenylethynyl)benzoate

https://huagongshe.com/reaction/1673394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantTriethylamineHCID 8471—
ReactantMethyl 2-(benzamido)-4-ethynylbenzoateHCID 57879399—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(benzamido)-4-(phenylethynyl)benzoateHCID 57879537—

Reaction Steps

1.5 mL of toluene suspension containing 0.15 g of methyl 2-(benzamido)-4-ethynylbenzoate, 0.090 mL of iodinated benzene, 5 mg of copper(I) iodide, 20 mg of bis(triphenylphosphine)palladium(II) chloride and 0.15 mL of triethylamine was stirred under nitrogen atmosphere at room temperature for 2 hours. Ethyl acetate and 1.0 mol/L hydrochloric acid were added to the reaction mixture. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium chloride aqueous solution, and the solvent was evaporated under reduced pressure. The obtained residue was purified with silica gel column chromatography [eluent; hexane:ethyl acetate=8:1] to obtain 0.13 g of methyl 2-(benzamido)-4-(phenylethynyl)benzoate as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-9ac1e5d467be4bf392af67f5c3694ac5
Source noteuspto-grants-2011_08