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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345038Generated: October 30, 2026

N-Ethylbenzylamine → N-Benzyl-N-ethyl-4-methanesulphonamidophenethylamine

https://huagongshe.com/reaction/345038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-EthylbenzylamineHCID 84352—
Reactant4-Methanesulphonamidophenethyl mesylateHCID 14985962—
SolventEthanolHCID 702—
ProductN-Benzyl-N-ethyl-4-methanesulphonamidophenethylamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055473
Source datasetuspto-grants-1991_10
ORD IDord-5c4f4c380bcd45009b0bb31ca061f0e8
Source noteuspto-grants-1991_10