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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799700Generated: October 31, 2026

Ethyl Acetate → 4-Ethoxycarbonyl-5-ethynylthiazole

https://huagongshe.com/reaction/1799700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTris(furan-2-yl)phosphaneHCID 521585—
ReactantEthynyltributyltinHCID 621176—
ReactantEthyl 5-iodothiazole-4-carboxylateHCID 59705069—
CatalystZincchlorideHCID 3007855—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventSodium chloride; waterHCID 57417360—
Product4-Ethoxycarbonyl-5-ethynylthiazoleHCID 59217960—

Reaction Steps

4-Ethoxycarbonyl-5-iodothiazole (1.45 g) was dissolved in 25 ml of N-methyl-2-pyrrolidinone. Tri-n-butylethynyltin (1.78 ml), 143 mg of tri(2-furyl)phosphine, 143 mg of tris(dibenzylideneacetone)dipalladium(0), and 1.43 g of zinc chloride were added to the solution under an argon atmosphere, and the mixture was stirred at room temperature for 40 min. Brine and ethyl acetate were added to the reaction solution. The insolubles were removed by filtration through Celite, and the filtrate was extracted twice with ethyl acetate. The organic layers were combined, were washed with brine, were dried over anhydrous magnesium sulfate, were filtered, and were concentrated under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=3:1) to give 750 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344154B2
Source datasetuspto-grants-2013_01
ORD IDord-91ca0aee4829420f884d7344a9da5883
Source noteuspto-grants-2013_01