HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 1-(4-Nitrobenzyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Nitrobenzyl)piperidine | HCID 783541 | — |
Reaction Steps
40.0 g of 4-nitrobenzyl bromide are dissolved in 500 ml of methylene chloride, 51.5 ml of triethylamine are added and 18.3 ml of piperidine are carefully added dropwise. After the end of the exothermic reaction the mixture is refluxed for another 30 minutes. After cooling it is washed with water and the organic phase is dried over sodium sulphate. Finally, the organic phase is evaporated down.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06762180B1 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-66caab325c4a46b2a247555427de3896 |
| Source note | uspto-grants-2004_07 |