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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383933Generated: October 31, 2026

Water → Ethyl 2,5'-bi-1,3-thiazole-4'-carboxylate

https://huagongshe.com/reaction/383933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-(Tributylstannyl)-1,3-thiazoleHCID 2763259—
ReactantEthyl 5-bromo-1,3-thiazole-4-carboxylateHCID 12361218—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
ProductEthyl 2,5'-bi-1,3-thiazole-4'-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367696B2
Source datasetuspto-grants-2013_02
ORD IDord-2d3cc926eced40e69b1b6f5f1e2d7c95
Source noteuspto-grants-2013_02