HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Fluoro-3-nitrobenzene → 1-Ethyl-4-(3-nitrophenyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Fluoro-3-nitrobenzene | HCID 9823 | — |
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 1-Ethyl-4-(3-nitrophenyl)piperazine | HCID 58235985 | — |
Reaction Steps
A mixture of 1-fluoro-3-nitrobenzene (3.2 mL, 29.7 mmol) and N-ethyl-piperazine (7.6 mL, 59.4 mmol, 2 equiv) is heated to reflux and stirred for 117 h. The reaction mixture is allowed to cool to RT and diluted with H2O (40 mL) and DCM/MeOH (9:1, 80 mL). The aqueous layer is separated and extracted with DCM/MeOH (9:1). The organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. Purification of the crude product by silica gel column chromatography (DCM/MeOH, 1:0-95:5) affords the title compound as a brown oil: ESI-MS: 236.0 [MH]+; tR=2.49 min (purity: 99%, system 1); TLC: Rf=0.26 (DCM/MeOH, 95:5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08293746B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-9589bc078a594381a18a2857b7901f29 |
| Source note | uspto-grants-2012_10 |