HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 1-((2-(Trifluoromethyl)phenyl)methyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(Bromomethyl)-2-(trifluoromethyl)benzene | HCID 123057 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-((2-(Trifluoromethyl)phenyl)methyl)piperazine | HCID 3023322 | 68.2% |
Reaction Steps
1.08 g (12.5 mmol) of piperazine are placed in the presence of 1 g (4.2 mmol) of 1-bromomethyl-2-trifluoromethyl-benzene and 0.64 mL (4.6 mmol) of triethylamine in 10 mL of toluene. The reaction medium is stirred for 30 min at room temperature and then heated to 110° C. for 6 h. After dry concentration, the obtained residue is taken up with AcOEt and washed with water. After drying on MgSO4, the organic phases are dry concentrated, the obtained residue is purified by flash chromatography on silica (CH2Cl2-MeOH—NH4OH: 90-9-1). 0.7 g of intermediate 7a are thereby isolated as a clear oil (yield 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08618287B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-4836326672db4340a251e84a74df417a |
| Source note | uspto-grants-2013_12 |