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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | Ethyl 5-bromo-1,3-thiazole-4-carboxylate | HCID 12361218 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Ethoxycarbonyl-5-(2-trimethylsilylethynyl)thiazole | HCID 59217954 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08344154B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-56b55940e5db49e3a165b8de5069d733 |
|---|
| Source note | uspto-grants-2013_01 |
|---|