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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440131Generated: October 31, 2026

Potassium Carbonate → (5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluoro-2-nitrophenyl)thio-acetic acid, ethyl ester

https://huagongshe.com/reaction/1440131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl ThioglycolateHCID 12185—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant4-chloro-3-(2,5-difluoro-4-nitrophenyl)-1-methyl-5-(trifluoromethyl)-1H-pyrazoleHCID 15278569—
SolventWaterHCID 962—
Product(5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluoro-2-nitrophenyl)thio-acetic acid, ethyl esterHCID 8674752043%

Reaction Conditions

Temperature28 °C

Reaction Steps

At 25° C., 1.5 g (4.5 mmole) 4-chloro-3-(2,5-difluoro-4-nitrophenyl)-1-methyl-5-(trifluoromethyl)-1H-pyrazole, 0.69 g (5.0 mmole) K2CO3, 0.55 mL (5.0 mmole) ethyl mercaptoacetate, and 0.05 g (0.5 mmole) CuF2 were slurried in 15 mL 1-methyl-2-pyrrolidinone. The reaction mixture was stirred 28° C. for 24 hours. The mixture was cooled, diluted with 100 mL cold water, and extracted four times with ethyl acetate. The ethyl acetate extracts were washed with brine, dried over anhydrous MgSO4, and stripped in vacuo. The residue was purified chromatographically using 10% diethyl ether and 15% methylene chloride in hexane as the eluent to give 0.86 g (43%) of (5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluoro-2-nitrophenyl)thio-acetic acid, ethyl ester as a yellow solid, mp 79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05496956
Source datasetuspto-grants-1996_03
ORD IDord-aedd61bb4ade446eb1ff4ca1a50594f6
Source noteuspto-grants-1996_03