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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103411Generated: October 31, 2026

Water → 1-(2,6-Dichloro-4-trifluoromethylphenyl)-3-cyano-5-(2-methoxyethylamino)-4-trifluoromethylsulfonylpyrazole

https://huagongshe.com/reaction/2103411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-MethoxyethylamineHCID 8018—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoromethylsulfonylpyrazoleHCID 16727054—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product1-(2,6-Dichloro-4-trifluoromethylphenyl)-3-cyano-5-(2-methoxyethylamino)-4-trifluoromethylsulfonylpyrazoleHCID 86599991—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 5-bromo-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoromethylsulfonylpyrazole (2.5 g, 4.8 mmol) in 1,4-dioxane and N,N-dimethylformamide was added 2-methoxyethylamine (0.74 g, 9.7 mmol) and potassium carbonate (1.35 g, 9.7 mmol). The resulting mixture was stirred at 50° C. for 4 hours, left to stand overnight, then poured into a mixture of water and dichloromethane. The organic phase was washed with water, dried (sodium sulfate), evaporated. The crude product was recrystallised from diisopropylether to give 1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-5-(2-methoxyethylamino)4-trifluoromethylsulfonylpyrazole as a white solid (Compound number 1-3, 1.30 g), mp 164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576107B2
Source datasetuspto-grants-2009_08
ORD IDord-3940b18768c54839b3e82b539ac291fe
Source noteuspto-grants-2009_08