Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54612Generated: October 26, 2026

Benzylethanolamine → Tert-butyl 2-(benzyl (2-hydroxyethyl)amino)acetate

https://huagongshe.com/reaction/54612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylethanolamineHCID 4348—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl bromoacetateHCID 79177—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 2-(benzyl (2-hydroxyethyl)amino)acetateHCID 15817339—

Reaction Steps

tert-Butyl bromoacetate (32.3 ml; 0.2 mol) is slowly added dropwise, while cooling in ice, to a solution of N-benzylethanolamine (30.2 g; 0.2 mol) and triethylamine (27.9 ml; 0.2 mol) in anhydrous N,N-dimethylformamide (200 ml). The mixture is stirred at room temperature for 22 h and is then concentrated in vacuo. The residue is subsequently distilled repeatedly with toluene. The resulting oil is taken up in dichloromethane (400 ml) and extracted twice by shaking with water (160 ml on each occasion). The organic phase is dried (magnesium sulphate) and concentrated. Yield: 47.8 g (90%), colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05623049
Source datasetuspto-grants-1997_04
ORD IDord-21aed8d69531446db839dc358717fabb
Source noteuspto-grants-1997_04