HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl[(2-nitrophenyl)methyl]amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | alpha-Bromo-2-nitrotoluene | HCID 77569 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl[(2-nitrophenyl)methyl]amine | HCID 14485081 | 100% |
Reaction Steps
2-Nitrobenzylbromide (0.23 mol) in tetrahydrofuran (500 ml) was added to a stirred mixture (4.35M) of 70% aqueous ethylamine (350 ml) and water (350 ml) over a 20 minutes. The reaction stood at ambient temperature for 1 hour, was reduced to low volume, treated with ice/water to 800 ml and basified with an aqueous solution of sodium hydroxide (1 ON, 23 ml). It was extracted with ether (2×) and the combined extracts dried (MgSO4) and evaporated to give N-ethyl-2-nitrobenzylamine as a yellow oil (44 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834468 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-2eb08fcffb8b4eba8533f9bd17e3f735 |
| Source note | uspto-grants-1998_11 |