Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799699Generated: November 1, 2026

Water → 4-Ethoxycarbonyl-5-(2-trimethylsilylethynyl)thiazole

https://huagongshe.com/reaction/1799699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantEthyl 5-bromo-1,3-thiazole-4-carboxylateHCID 12361218—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product4-Ethoxycarbonyl-5-(2-trimethylsilylethynyl)thiazoleHCID 59217954—

Reaction Conditions

Temperature90 °C

Reaction Steps

5-Bromo-4-ethoxycarbonylthiazole (18.64 g) was dissolved in 80 ml of DMF. Triethylamine (22 ml), 16.7 ml of ethynyltrimethylsilane, 960 mg of copper(I) iodide, and 1.11 g of bis(triphenylphosphine)palladium(II) dichloride were added in that order to the solution, and the mixture was stirred at 90° C. under an argon atmosphere for one hr. Water (80 ml), 160 ml of ethyl acetate and 160 ml of hexane were added to the reaction solution, and the mixture was washed with (brine+aqueous hydrochloric acid), sodium bicarbonate water, and brine in that order. Activated carbon and anhydrous magnesium sulfate were added to the organic layer, and the mixture was filtered and was concentrated under the reduced pressure to give 16.45 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344154B2
Source datasetuspto-grants-2013_01
ORD IDord-56b55940e5db49e3a165b8de5069d733
Source noteuspto-grants-2013_01