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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130266Generated: October 26, 2026

Hydrochloric Acid → Stearyl Pyridone

https://huagongshe.com/reaction/130266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl cyanoacetateHCID 7764—
ReactantPiperidineHCID 8082—
ReactantEthyl AcetoacetateHCID 8868—
ReactantOctadecylamineHCID 15793—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductStearyl PyridoneHCID 8660527165.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

Into a 2 liter Erlenmeyer flask equipped with magnetic stirring was charged stearylamine (118 g, 0.44 mol; obtained from Sigma-Aldrich) and ethyl cyanoacetate (ECA, 45.2 grams, 0.4 mol). The mixture was heated to 120° C. for 90 minutes, after which ethyl acetoacetate (EAA, 114 grams, 0.88 mol), piperidine (PIP; 70 grams, 0.82 mol), and dimethylformamide (DMF; 140 milliliters) were added. The mixture was heated to 120° C. for 4 hours. The mixture was then allowed to cool to room temperature and was poured slowly into well stirred methanol (1,200 milliliters), which contained concentrated hydrochloric acid (100 milliliters). The resulting suspension was allowed to stir for 10 minutes, and was then filtered and washed with 3×200 milliliter portions of methanol. The resulting solid was oven dried at 60° C. to give 91.3 grams of a beige powder at 57 percent yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381253B2
Source datasetuspto-grants-2008_06
ORD IDord-2302910246ad4d5996efcd7c909db375
Source noteuspto-grants-2008_06