HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Methyl-4-(4-nitro-2-(trifluoromethyl)benzyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(Bromomethyl)-4-nitro-2-(trifluoromethyl)benzene | HCID 46838761 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Methyl-4-(4-nitro-2-(trifluoromethyl)benzyl)piperazine | HCID 46838906 | 72.9% |
Reaction Steps
To a solution of crude 1-(bromomethyl)-4-nitro-2-(trifluoromethyl)benzene (13.33 mmol, 75% pure) in DCM (10 mL) was added Et3N (1.4 mL, 10 mmol) and 1-methylpiperazine (1.1 mL, 10 mmol). After stirring for 3 h at rt, aq. NaHCO3 was added, and the mixture was extracted with DCM. The combined organic layer was dried over Na2SO4, filtered, concentrated, and the resulting residue was purified by silica gel chromatography (eluted with 10% MeOH/DCM) to provide 2.21 g of product as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461167B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-c08f576b34d54dfab3a3c435e02b7bb7 |
| Source note | uspto-grants-2013_06 |