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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607905Generated: October 30, 2026

5-(Trifluoromethyl)isoxazole → HCID 14280193, compound

https://huagongshe.com/reaction/1607905

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Trifluoromethyl)isoxazoleHCID 4463981—
ReactantSodiumHCID 5360545—
ReactantHCID 19849800HCID 19849800—
SolventEthanolHCID 702—
ProductHCID 14280193HCID 142801939.3%

Reaction Steps

0.92 g (0.04 mol) of sodium is dissolved in 25 ml of ethanol, 5.48 g (0.04 mol) of 5-trifluoromethylisoxazole are added at 0° C. and the mixture is stirred at room temperature for 15 minutes. 16.16 g (0.04 mol) of N-(2,6-dichloro-4-trifluoromethylphenyl)-trifluoroacetohydrazide bromide are added dropwise to this mixture, while cooling, and the mixtureis subsequently stirred at 25° C. for a further 10 hours. After the sodium bromide which has precipitated out is filtered off, the filtrate isconcentrated and the residue is separatad by column chromatography. 1.65 g (9.3% of theory) of 4-cyano-3,5-di(trifluoromethyl)-1-(2,6-dichloro-4-trifluoromethylphenyl)-pyrazole of melting point 88° C.-92° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868198
Source datasetuspto-grants-1989_09
ORD IDord-f9be40d72b89460e8bbf19c63f0c6b9d
Source noteuspto-grants-1989_09