HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-Amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1H-Pyrazol-3-amine, 5-methyl- | HCID 93146 | — |
| Reactant | alpha-Chloro-3-nitrobenzaldoxime | HCID 2756318 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazole | HCID 73508416 | 75% |
Reaction Steps
4.85 g (0.05 mol) of 3(5)-amino-5(3)-methyl-pyrazole in 50 ml of absolute dioxan are treated with 8.3 ml (0,06 mol) of triethylamine and then, under stirring at room temperature, are treated dropwise with a solution of 10 g (0.05 mol) of 3-nitro-benzohydroximoyl chloride in 50 ml of absolute dioxan. Stirring is continued for 3 hours and then the mixture is evaporated to dryness. The residue is treated with water and ethyl acetate. The organic phase is dried over magnesium sulphate, evaporated under vacuum and the residue obtained in this way is recrystallised from dioxan. 9.8 g (48%) of 5-amino-1-(3-nitro-benzohydroximoyl)-3-methyl-pyrazole with a m. pt. of 224° to 226° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05336780 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-9951e2f903c54e1da04e592485a75fc4 |
| Source note | uspto-grants-1994_08 |