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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918770Generated: November 1, 2026

Potassium Carbonate → Ethyl 2-[3-(3,4,5-trichlorophenyl)-3-(trifluoro-methyl)pyrrolidin-1-yl]-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/918770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylateHCID 1235240—
Reactant3-(3,4,5-Trichlorophenyl)-3-(trifluoromethyl)pyrrolidineHCID 59453372—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-[3-(3,4,5-trichlorophenyl)-3-(trifluoro-methyl)pyrrolidin-1-yl]-4-(trifluoromethyl)-1,3-thiazole-5-carboxylateHCID 5945336586.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

Ethyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate (1.4 g) [see J. Het. Chem., 22, 1621 (1985)], 3-(3,4,5-trichlorophenyl)-3-(trifluoromethyl)pyrrolidine (1.7 g), and potassium carbonate (0.8 g) were added to N,N-dimethylformamide (50 mL), followed by heating at 100° C. for five hours. After cooling, the reaction solution was poured over ice water, and then extracted with ethyl acetate. The organic layer was dried over magnesium sulfate. The solvent was evaporated off under reduced pressure, and the residue was then purified by a silica gel chromatography to obtain the title compound (2.5 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09271499B2
Source datasetuspto-grants-2016_03
ORD IDord-24945c868ee545f8bff1fe7849701947
Source noteuspto-grants-2016_03