HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → [2-(4-Methylpiperazino)-5-nitrophenyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | (2-Fluoro-5-nitrophenyl)methanol | HCID 4437169 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [2-(4-Methylpiperazino)-5-nitrophenyl]methanol | HCID 25918812 | 94% |
Reaction Steps
2-Fluoro-5-nitrobenzyl alcohol (1 g, 5.84 mmol) and N-methylpiperazine (1.29 mL, 2 eq) were heated at 130° C. for 1 h. The reaction mixture was then diluted with 25 mL of THF and washed with a saturated aqueous solution of Na2CO3 and then with brine. The organic layer was dried over Na2SO4, filtered and evaporated. The residue was thoroughly washed with pentane and filtered off to yield expected compound as an orange powder (1.38 g, 94% yield). m/z (ESI) 252.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680095B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-a7a4d715d5a94319bcd29bd81c8f21d4 |
| Source note | uspto-grants-2014_03 |