Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5247Generated: October 26, 2026

Hydrochloric Acid → HCID 178418643, compound

https://huagongshe.com/reaction/5247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantPalmitoleic AcidHCID 445638—
ReactantTetronic acidHCID 521261—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventEthylacetate methanolHCID 21584119—
ProductHCID 178418643HCID 17841864336%

Reaction Steps

To a stirring solution of 1.07 g (10.72 mmol) of tetronic acid in 30 mL of dimethylformamide is added 1.64 mL (11.97 mmol) of triethylamine and 428 mg of 4-dimethylaminopyridine at 0° C. Next, 2.44 g (12.77 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 3.0 g (11.79 mmol) of palmitoleic acid are added and the reaction is stirred for 3 days at room temperature. The reaction is acidified with 1.0N HCl and extracted with four 100 mL portions of ethyl acetate. The combined organic layers are dried over MgSO4 and concentrated in vacuo affording crude compound. Pure material was obtained by flash chromatography with 10% methanol/ethyl acetate as eluant affording 1.3 g (36%) of 4-hydroxy-3-((Z)-1-oxo-9-hexadecenyl)-2(5H)-furanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05242945
Source datasetuspto-grants-1993_09
ORD IDord-a7cf8eaa48de44358d5af939538ff052
Source noteuspto-grants-1993_09