HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Ethyl-4-(2-methyl-4-nitro-benzyl)-piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Reactant | 1-(Bromomethyl)-2-methyl-4-nitrobenzene | HCID 12654147 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Ethyl-4-(2-methyl-4-nitro-benzyl)-piperazine | HCID 67457996 | — |
Reaction Steps
A solution of 1 g (3.78 mmol) 1-bromomethyl-2-methyl-4-nitro-benzene, 0.539 ml (4.16 mmol) 1-ethylpiperazine and 0.63 ml (4.54 mmol) triethylamine in 15 ml dichloromethane is stirred at room temperature for 0.5 h. Then the reaction mixture is poured on water and extracted 3× with EtOAc. The combined organic layers are washed with water and saturated NaCl solution, dried over MgSO4, filtered and the filtrate is concentrated in vacuo. The residue is purified by chromatography (silicagel, 100% EtOAc=>EtOAc:MeOH=7:3) to afford the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08629168B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-8b37891adf07410fa7861fde38845bf9 |
| Source note | uspto-grants-2014_01 |