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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776988Generated: November 3, 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/1776988

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 numberUS09266830B2
Source datasetuspto-grants-2016_02
ORD IDord-53437cd73c6d4e55a02fa04595183111
Source noteuspto-grants-2016_02