HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Ethylbenzylamine → N-Benzyl-N-ethyl-4-methanesulphonamidophenethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Ethylbenzylamine | HCID 84352 | — |
| Reactant | 4-Methanesulphonamidophenethyl mesylate | HCID 14985962 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-Benzyl-N-ethyl-4-methanesulphonamidophenethylamine | HCID 19813439 | — |
Reaction Steps
4-Methanesulphonamidophenethyl mesylate (10 g, 34 mmole) and N-ethylbenzylamine (10 ml, 67 mmole) were heated at reflux temperature in ethanol (80 ml) for 3 hours. The solvent was evaporated, the residue taken up in 2M hydrochloric acid and washed twice with methylene chloride. The aqueous layer was basified with sodium bicarbonate (to pH~12) and extracted with methylene chloride. The latter organic extract was dried (MgSO4) and evaporated to give an oil which solidified when triturated with diisopropyl ether. The solid was filtered off and discarded and the filtrate was evaporated in vacuo to give the title compound as an oil, yield 4.4 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05158964 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-92e468445f10429abc57c1129187eaf2 |
| Source note | uspto-grants-1992_10 |