HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(Trifluoromethyl)isoxazole → HCID 14280193, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(Trifluoromethyl)isoxazole | HCID 4463981 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 19849800 | HCID 19849800 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14280193 | HCID 14280193 | 9.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868198 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-f9be40d72b89460e8bbf19c63f0c6b9d |
| Source note | uspto-grants-1989_09 |