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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401136Generated: October 25, 2026

Ethyl benzoate → 1-Phenyl-2-(thiazol-2-yl)ethanone

https://huagongshe.com/reaction/401136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl benzoateHCID 7165—
ReactantEthyl AcetateHCID 8857—
Reactant2-MethylthiazoleHCID 77129—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-Phenyl-2-(thiazol-2-yl)ethanoneHCID 1788704717%

Reaction Steps

To a solution of 2-methylthiazole (500 mg, 5.1 mmol) in anhydrous THF (10 mL) at −78° C. under nitrogen was added dropwise n-BuLi (2.5 mol/L, 2.0 mL), after being stirred at this temperature for 1 hour, a solution of ethyl benzoate (1.1 g, 7.3 mmol) in anhydrous THF (5 mL) was added, and the reaction mixture was stirred at room temperature overnight. When TLC (PE:EtOAc=7:1) indicated that the starting materials were consumed, water was added to quench the reaction, and the aqueous layer extracted with EtOAc (10 mL×3). The combined organic layer was washed with brine (10 mL), dried over Na2SO4, filtered, concentrated, and purified by column chromatography (PE:EtOAc=15:1) to afford Intermediate 3 as a yellow oil (170 mg, yield: 17.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741915B2
Source datasetuspto-grants-2014_06
ORD IDord-80d7ee6addf34ef69dbb850eebd5c724
Source noteuspto-grants-2014_06