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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260950Generated: October 29, 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/260950

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 numberUS05530126
Source datasetuspto-grants-1996_06
ORD IDord-f93bab6812724401809ff92167ccf1f1
Source noteuspto-grants-1996_06