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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530760Generated: October 30, 2026

Ethyl Acetate → Ethyl 3-oxo-3-(4-(trifluoromethyl)thiazol-2-yl)propanoate

https://huagongshe.com/reaction/530760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantEthyl 4-(trifluoromethyl)thiazole-2-carboxylateHCID 23560697—
ReactantHCID 178418922HCID 178418922—
SolventTolueneHCID 1140—
ProductEthyl 3-oxo-3-(4-(trifluoromethyl)thiazol-2-yl)propanoateHCID 6816009545%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 4-trifluoromethylthiazole-2-carboxylic acid ethylester (8.88 mmol) in toluene (50 mL) were added successively EtOAc (13.32 mmol) and tBuOK (17.76 mmol). The resulting mixture was stirred at 100° C. for 1 hr. The solvent was removed by evaporation and water and Et2O were added. The solution was neutralized with acetic acid. The extract was washed with water and the organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure to give compound 28 as a yellow oil in 45% yield. MS (ESI, EI−): m/z=266 (MH−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353100B2
Source datasetuspto-grants-2016_05
ORD IDord-145880d0f7ac4c79a88cda401751ec9f
Source noteuspto-grants-2016_05