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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353676Generated: October 25, 2026

Hydrochloric Acid → 2-Ethylhexyl pyridone

https://huagongshe.com/reaction/353676

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 numberUS06755902B2
Source datasetuspto-grants-2004_06
ORD IDord-364aed43fef1480284ccd1eda5d3c21e
Source noteuspto-grants-2004_06