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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467237Generated: October 26, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-(2-(benzyloxy)ethyl)-3-hydroxy-2,2-dimethylpropanamide

https://huagongshe.com/reaction/1467237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Hydroxy-2,2-dimethylpropionic acidHCID 78548—
Reactant2-(Benzyloxy)ethanamineHCID 533868—
SolventDichloromethaneHCID 6344—
ProductN-(2-(benzyloxy)ethyl)-3-hydroxy-2,2-dimethylpropanamideHCID 6674596497.3%

Reaction Steps

To a solution of 3-hydroxy-2,2-dimethylpropanoic acid (2.36 g, 20 mmol), 2-(benzyloxy)ethanamine (3.02 g, 20 mmol), and HOBt (2.71 g, 20 mmol) in dry dichloromethane (100 mL) was added EDCI (3.82 g, 20 mmol) at room temperature under nitrogen. The reaction mixture was then stirred at room temperature under nitrogen overnight. The reaction was quenched with brine, and extracted with EtOAc (3×). The combined organic layers were washed with saturated NaHCO3 solution, dilute HCl, brine, and dried over Na2SO4. After evaporation of the solvent, the residue was purified by chromatography on silica gel eluting with 40% EtOAc in hexanes to give the title compound as colorless oil (4.89 g) in 97% yield. MS 252 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000054B2
Source datasetuspto-grants-2015_04
ORD IDord-6fd75d21e31b4a0dbb3fecbac9cdd79e
Source noteuspto-grants-2015_04