HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 2,5'-bi-1,3-thiazole-4'-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(Tributylstannyl)-1,3-thiazole | HCID 2763259 | — |
| Reactant | Ethyl 5-bromo-1,3-thiazole-4-carboxylate | HCID 12361218 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 2,5'-bi-1,3-thiazole-4'-carboxylate | HCID 59291355 | — |
Reaction Steps
To a solution of ethyl 5-bromo-1,3-thiazole-4-carboxylate in toluene were added 2-(tributylstannyl)-1,3-thiazole and PdCl2(PPh3)2, followed by heating under reflux for 6 hours. Water was added thereto and the aqueous layer was extracted with EtOAc. The organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by medium-pressure preparative liquid chromatography (silica gel, YAMAZEN YFLC WPrep2XY, hexane: EtOAc) to obtain ethyl 2,5′-bi-1,3-thiazole-4′-carboxylate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367696B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-2d3cc926eced40e69b1b6f5f1e2d7c95 |
| Source note | uspto-grants-2013_02 |