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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236511Generated: October 31, 2026

Triethylamine → HCID 53724108, compound

https://huagongshe.com/reaction/236511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant3-Hexadecanoyloxyoctadecanoic acidHCID 13489028—
ReactantHCID 54173537HCID 54173537—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 53724108HCID 5372410881.5%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of 3-hexadecanoyloxyoctadecanoic acid (55 g) and triethylamine (16 ml) in tetrahydrofuran (500 ml) was added ethyl chloroformate (11 ml) dropwise with stirring at -20° C., and the mixture was stirred for 1 hour at the same temperature. To the mixture was added triethylamine (32 ml) and then, a solution of dibenzyl N-(L-threonyl)-L-glutamate (77 g) in tetrahydrofuran (100 ml) dropwise and the mixture was stirred for 3 hours at room temperature. Tetrahydrofuran was removed under reduced pressure to give the residue which was taken up in ethyl acetate. The ethyl acetate solution was washed with diluted hydrochloric acid and diluted sodium bicarbonate and dried. Evaporation of the solvent gave the residue which was recrystallized from ethanol to leave dibenzyl N-[N-(3-hexadecanoyloxyoctadecanoyl)-L-threonyl]-L-glutamate (79 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04643990
Source datasetuspto-grants-1987_02
ORD IDord-6165d32b79f6434aa7c9acfe679dbac3
Source noteuspto-grants-1987_02