HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 1-(3-methyl-4-nitrobenzyl)-5-pentafluoroethyl-1H-pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 5-Ethoxy-1,1,1,2,2-pentafluoro-4-penten-3-one | HCID 3729085 | — |
| Reactant | [(3-Methyl-4-nitrophenyl)methyl]hydrazine | HCID 20367228 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(3-methyl-4-nitrobenzyl)-5-pentafluoroethyl-1H-pyrazole | HCID 86076299 | — |
| Product | 1-(3-methyl-4-nitrobenzyl)-3-pentafluoroethyl-1H-pyrazole | HCID 86076301 | — |
Reaction Steps
(3-Methyl-4-nitrobenzyl)-hydrazine (1.81 g) and 5-ethoxy-1,1,1,2,2-pentafluoro-4-penten-3-one (2.18 g) were refluxed in ethanol (60 ml) for 8 hours, and p-toluenesulfonic acid (0.10 g) was added thereto and the mixture was further refluxed for 6 hours. After finishing the reaction, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography (mixed solvent of n-hexane and ethyl acetate) to obtain 1-(3-methyl-4-nitrobenzyl)-5-pentafluoroethyl-1H-pyrazole (0.96 g) as the first elution portion and 1-(3-methyl-4-nitrobenzyl)-3-pentafluoroethyl-1H-pyrazole (0.50 g) as the second elution portion.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07674807B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-b0e3e501ad744800bac8c0722182f726 |
| Source note | uspto-grants-2010_03 |