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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187898Generated: November 1, 2026

Thiazole → HCID 22716763, compound

https://huagongshe.com/reaction/2187898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazoleHCID 9256—
Reactant4-(Methylthio)benzaldehydeHCID 76985—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22716763HCID 22716763—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a −78° C. solution of thiazole (5.0 g, 58.7 mmol) in THF (250 ml) was added n-butyllithium (2.5M in hexanes, 23.5 ml, 58.7 mmol) dropwise and the resulting solution was stirred at −78° C. for 10 min. 4-(Methylthio)benzaldehyde (7.1 ml, 53.4 mmol) was then added at −78° C. The resulting mixture was stirred until completion, and quenched with a saturated aqueous solution of NH4Cl. The mixture was then diluted with EtOAc and HCl 10%, extracted and washed (NaHCO3 (sat.), brine). The organic phase was dried over MgSO4 and concentrated. The residue was then purified by flash chromatography (80% CH2Cl2/20% EtOAc) to yield (1,3-Thiazol-2-yl)[4-(methylthio)phenyl]methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410563B1
Source datasetuspto-grants-2002_06
ORD IDord-2b6d8b44fefc4fbc9e9c7161db384a32
Source noteuspto-grants-2002_06