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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414336Generated: October 30, 2026

Ammonia → HCID 13561854, compound

https://huagongshe.com/reaction/414336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPyridineHCID 1049—
ReactantPropionyl chlorideHCID 62324—
Reactant5-Amino-4-cyano-1-(2-chloro-4-trifluoromethoxy-phenyl)-pyrazoleHCID 13561833—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
ProductHCID 13561854HCID 1356185475.3%

Reaction Steps

10 ml (0.11 mole) of propionyl chloride are added to 2.9 g (0.01 mole) of 5-amino-4-cyano-1-(2-chloro-4-trifluoromethoxy-phenyl)-pyrazole in 30 ml of chloroform at 0° C., with stirring, and a solution of 1.8 ml (0.02 mole) of pyridine in 15 ml of chloroform is then added, also at 0° C. When the addition has ended, stirring is continued at room temperature for 20 hours, the solvent is stripped off, the residue is taken up in 50 ml of ethanol, aqueous ammonia is added until the reaction is alkaline, the volatile constituents are removed in vacuo, the residue is taken up in 100 ml of chloroform, the mixture is washed with water, then with 2N aqueous hydrochloric acid and again with water and dried over sodium sulphate and the solvent is removed in vacuo. 2.7 g (75.3% of theory) of 4-cyano-1-(2-chloro-4-trifluoromethoxy-phenyl)-5-propionylamino-pyrazole of melting point 127° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04791212
Source datasetuspto-grants-1988_12
ORD IDord-89981ef22669433c97efbf4f519c8732
Source noteuspto-grants-1988_12