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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236481Generated: October 25, 2026

Hydrochloric Acid → N-[3-(Hexadecanoyloxy)octadecanoyl]-L-valine

https://huagongshe.com/reaction/236481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantL-ValineHCID 6287—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant3-Hexadecanoyloxyoctadecanoic acidHCID 13489028—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Solvent1,4-DioxaneHCID 31275—
ProductN-[3-(Hexadecanoyloxy)octadecanoyl]-L-valineHCID 5372993762.6%

Reaction Steps

3-Hexadecanoyloxyoctadecanoic acid (10.8 g) prepared by the method described in Preparation A-2 (5) and N-hydroxysuccinimide (2.3 g) was dissolved in dioxane (60 ml). N,N'-Dicyclohexylcarbodiimide (4.2 g) was added thereto under ice cooling. The mixture was stirred at ambient temperature over-night. The crystallized N,N'-dicyclohexylurea was filtered off and the filtrate was concentrated to give a residue. The residue was dissolved in N,N-dimethylformamide (70 ml). To this solution was added a solution of L-valine (5.85 g) and triethylamine (6.95 ml) in water (50 ml) at 0° C. The resulting mixture was stirred at ambient temperature overnight. The reaction mixture was acidified with 1N hydrochloric acid, extracted with ethyl acetate, washed with water and dried over magnesium sulfate. Ethyl acetate was distilled off to give a residue which was crystallized from petroleum ether to give crystals of N-(3-hexadecanoyloxyoctadecanoyl)-L-valine (8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04643990
Source datasetuspto-grants-1987_02
ORD IDord-8f9b83e64f3f4693b46e3b73e9a3fec2
Source noteuspto-grants-1987_02