Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407050Generated: October 30, 2026

Stearic Acid → Methyl 3-oxoicosanoate

https://huagongshe.com/reaction/2407050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStearic AcidHCID 5281—
ReactantTriethylamineHCID 8471—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantDiethyl cyanophosphonateHCID 76257—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-oxoicosanoateHCID 84502—

Reaction Steps

Stearic acid (5.0 g, 17.6 mmoles) is suspended in methylene chloride (88 mL) and 2,2-dimethyl-1,3-dioxane-4,6-dione (2.7 g, 18.5 mmoles), triethylamine (6.7 mL, 48.0 mmoles) and diethyl cyanophosphonate (2.7 mL, 17.6 mmoles) are added. All solids dissolve quickly. The solution is stirred for 16 hours at ambient temperature. The reaction mixture is then diluted with methylene chloride (100 mL) and carefully washed three times with aqueous hydrochloric acid (3 M, 50 mL each), three times with water (50 mL each) and once with saturated aqueous sodium chloride (50 mL). The reaction mixture is then dried over anhydrous sodium sulfate, filtered and evaporated. The resulting syrup is dissolved in anhydrous methanol (100 mL) and heated to reflux for 16 hours. The methanol is evaporated and the crude product dissolved in hexanes with slight heating. The crude product was then loaded on silica gel (150 mL bed volume) eluting with hexanes (500 mL) then hexane:acetone (98:2 [v/v], 1000 mL). Fractions containing pure product by thin layer chromatography are pooled and evaporated to dryness. The resulting oil is dried well in vacuo. The yield is 5.2 g (87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809514B2
Source datasetuspto-grants-2014_08
ORD IDord-81d350cd002140cf9d0f94ef01ad7bdc
Source noteuspto-grants-2014_08