HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695517Generated: November 2, 2026
Potassium Carbonate → Ethyl 2-(3-methanesulphonylphenyl)thiazole-4-carboxylate
https://huagongshe.com/reaction/1695517
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-bromo-1,3-thiazole-4-carboxylate | HCID 353965 | — |
| Reactant | 3-(Methylsulfonyl)phenylboronic acid | HCID 2773542 | — |
| Catalyst | HCID 178456358 | HCID 178456358 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 2-(3-methanesulphonylphenyl)thiazole-4-carboxylate | HCID 67277205 | 47.7% |
Reaction Steps
Ethyl 2-bromothiazole-4-carboxylate (1 g), 3-(methylsulphonyl)phenyl-boronic acid (1.02 g, 1.2 equivalents) and potassium carbonate (1.76 g) are introduced in dioxane (12.5 ml). (1,3-Diisopropylimidazol-2-ylidene)(3-chloropyridyl)palladium(II) dichloride (288 mg) is added, and the mixture is stirred under reflux under protective gas for 18 h. Dioxane is then removed in a rotary evaporator, and the residue is taken up in ethyl acetate and water. The organic phase is separated off and the aqueous phase is back-extracted twice with ethyl acetate. The combined organic phases are washed with brine and dried over sodium sulphate and concentrated. Purification by column chromatography on silica gel (ethyl acetate/hexane) results in a white solid (629 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08163739B2 |
|---|
| Source dataset | uspto-grants-2012_04 |
|---|
| ORD ID | ord-75f1eea9453248d1a790e15de0fcd9c2 |
|---|
| Source note | uspto-grants-2012_04 |
|---|