HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Ethyl-2,5-difluoro-4-(4-methyl-1-piperazinyl)nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 3-Ethyl-2,4,5-trifluoro-nitrobenzene | HCID 14834677 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3-Ethyl-2,5-difluoro-4-(4-methyl-1-piperazinyl)nitrobenzene | HCID 19841121 | — |
Reaction Steps
To 3-ethyl-2,4,5-trifluoro-nitrobenzene (1.02 g) are added ethanol (4.5 ml) and water (0.5 ml) and the mixture is stirred. To the mixture is added with stirring a mixture of 1-methylpiperazine (0.83 ml), triethylamine (1.0 ml) and ethanol (0.6 ml), and the mixture is refluxed for 5 hours. To the reaction mixture is further added 1-methylpiperazine (1.0 ml), and the mixture is refluxed for 3 hours. The mixture is concentrated under reduced pressure, and the resulting residue is purified by silica gel column chromatography (solvent, methylene chloride) to give 3-ethyl-2,5-difluoro-4-(4-methyl-1-piperazinyl)nitrobenzene (1.12 g), as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04880806 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-2f346a1d8b1d4149993b9b2ac168d393 |
| Source note | uspto-grants-1989_11 |