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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198409Generated: October 30, 2026

Potassium Carbonate → 5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluoro-N-methyl-2-nitro-N-propylbenzenamine

https://huagongshe.com/reaction/1198409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-MethylpropylamineHCID 12315—
Reactant4-chloro-3-(2,5-difluoro-4-nitrophenyl)-1-methyl-5-(trifluoromethyl)-1H-pyrazoleHCID 15278569—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluoro-N-methyl-2-nitro-N-propylbenzenamineHCID 1527857686.1%

Reaction Conditions

Temperature35 °C

Reaction Steps

At 25° C., 6.83 g (0.02 mole) 4-chloro-3-(2,5-difluoro-4-nitrophenyl)-1-methyl-5-(trifluoromethyl)-1H-pyrazole, 4.1 g (0.03 mole) K2CO3, 3.1 mL (0.03 mole) N-methyl-N-propylamine and a catalytic amount of CuF2 were slurried in 50 mL 1-methyl-2-pyrrolidinone. The reaction mixture was stirred at 35° C. for 2 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 15% ethyl acetate in hexane as the eluent to give 6.8 g (86%) of 5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluoro-N-methyl-2-nitro-N-propylbenzeneamine as an orange oil, nD25 1.5534.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281571
Source datasetuspto-grants-1994_01
ORD IDord-6f637398e3f3431595481c2dddc5ccd6
Source noteuspto-grants-1994_01