Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429247Generated: October 27, 2026

Water → 5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-pyrazolecarboxamide oxime

https://huagongshe.com/reaction/429247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrileHCID 3303913—
Solvent1,4-DioxaneHCID 31275—
Product5-Amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-pyrazolecarboxamide oximeHCID 13636424775.2%

Reaction Steps

5-Amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)pyrazole (10.0 g, 31.1 mmol) was dissolved in 150 ml of dry dioxane, and then hydroxylamine hydrochloride (3.35 g, 46.8 mmol) and triethylamine (6.6 ml, 47.4 mmol) were added with stirring at room temperature. The mixture was stirred at room temperature for 74 hours and the reaction solution was poured into 300 ml of iced water. The solution was stirred for 30 minutes and the deposited crystal was filtered. The resulting crystal was washed with water and then dried under reduced pressure to obtain 8.30 g (23.4 mmol) of the title compound as a colorless crystal. The aqueous layer obtained by combining the above filtrate and wash was extracted three times with 150 ml of ethyl acetate. The extracted solution was washed three times with 500 ml of an aqueous saturated sodium chloride solution and the organic layer was dried over anhydrous magnesium sulfate. After concentrating under reduced pressure, the resulting crystal was washed with 50 ml of chloroform-hexane (1:1) and then filtered to obtain 1.19 g (3.36 mmol) of the title compound as a pale brown crystal. Yield 86%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316477B1
Source datasetuspto-grants-2001_11
ORD IDord-0bd22c53dfc54b23b66e1d440dd7c726
Source noteuspto-grants-2001_11