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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757862Generated: November 1, 2026

Sodium Iodide → Glycine [[bis(2-hydroxyethyl)amino]carbonyl]methyl ester

https://huagongshe.com/reaction/1757862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChloroacetyl chlorideHCID 6577—
ReactantDiethanolamineHCID 8113—
ReactantTriethylamineHCID 8471—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(carboxymethyl)-N-(3,5-bis(decyloxy)-phenyl)glycineHCID 192621—
Reactant2-chloro-N,N-bis(2-hydroxyethyl)acetamideHCID 350565—
SolventDimethylformamideHCID 6228—
ProductGlycine [[bis(2-hydroxyethyl)amino]carbonyl]methyl esterHCID 131718524—

Reaction Steps

A mixture of 1.0 g (1.92 mmol) of N-(carboxymethyl)-N-[3,5-bis(decyloxy)phenyl]glycine, 2.6 ml of N,N-diisopropylethylamine and a solution of N,N-bis(2-hydroxyethyl)-2-chloroacetamide [prepared from the reaction of 2.1 g (20 mmol) of diethanolamine, 1.6 ml (20 mmol) of chloroacetyl chloride and 3.1 ml (22 mmol) of triethylamine in 25 ml of DMF] was stirred at room temperature for 17 hours. Sodium iodide (3.0 g, 20 mmol) was added and the reaction mixture was stired and heated at 60° under argon for 25 hours. The mixture was concentrated at reduced pressureand NaHCO3 solution was added to the residue. The product was extracted with ethyl acetate and the extract was washed with water, dried and concentrated to an oil which was crystallized from methylene chloride-ether to give 0.455 g (29% yield, mp 104°-107°) of N-[3,5-bis(decyloxy)phenyl]-N-[[bis(2-hydroxyethyl)amino]carbonyl]methoxy]-2-oxoethyl]glycine [[bis(2-hydroxyethyl)amino]carbonyl]methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446189
Source datasetuspto-grants-1995_08
ORD IDord-2aefb82821eb4abd94b03d4a13ef5e17
Source noteuspto-grants-1995_08