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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357323Generated: October 26, 2026

Hydrochloric Acid → 2-Ethylhexyl pyridone

https://huagongshe.com/reaction/1357323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-EthylhexylamineHCID 7719—
ReactantMethyl cyanoacetateHCID 7747—
ReactantPiperidineHCID 8082—
ReactantEthyl AcetoacetateHCID 8868—
SolventMethanolHCID 887—
Product2-Ethylhexyl pyridoneHCID 8659072982%

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a 1 liter round-bottom flask equipped with stirrer and Dean Stark trap was charged methyl cyanoacetate (99 grams, 1 mol; obtained from Sigma-Aldrich Co., Milwaukee, Wis.), followed with methanol solvent (150 milliliters), and the mixture was stirred briefly. 2-Ethylhexylamine (130 grams, 1 mol) was slowly added into this mixture, followed with the sequential addition of ethyl acetoacetate (130 grams, 1 mol; obtained from Sigma-Aldrich Co.), and then piperidine (85 grams, 1 mol; obtained from Sigma-Aldrich Co.). The solution was stirred and heated at 100° C. for 12 hours, and then was cooled to room temperature. The mixture was diluted with 2,500 milliliters of methanol and acidified carefully with concentrated hydrochloric acid until a large amount of precipitate had formed. The precipitate was filtered by vacuum and repeatedly washed with deionized water and filtered until the filtrate was of neutral pH. The crude material was recrystallized in warm methanol to afford 170 grams (65 percent yield) of 2-ethylhexyl pyridone as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06590082B1
Source datasetuspto-grants-2003_07
ORD IDord-0fa9d38c24c04401b0e1927af028f02b
Source noteuspto-grants-2003_07