Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296344Generated: November 1, 2026

Diethyl Oxalate → HCID 54347591, compound

https://huagongshe.com/reaction/2296344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantTetradecanenitrileHCID 64678—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductHCID 54347591HCID 54347591—

Reaction Steps

0.5 Moles of n-tridecyl cyanide and 0.5 moles of diethyl oxalate are mixed in 1,000 ml of dimethylformamide. To this solution is added with ice cooling 0.52 moles of potassium t-butoxide. The mixture is allowed to stir overnight at room temperature. Following evaporation (rotary evaporator under vacuum) of most of the dimethylformamide the residue is mixed with 3 liters of diethyl ether followed by the addition of 1 liter water. The mixture is acidified with concentrated hydrochloric acid to a pH of 3 and then the ether phase is separated. After washing the ether with water and drying the ether over magnesium sulfate evaporation of the ether affords 3-cyano-2-oxopentadecanoic acid ethyl ester. Recrystallization from petroleum ether at 30°-60° C. provides pure material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04428959
Source datasetuspto-grants-1984_01
ORD IDord-35b8f197ac6e45c698b5aec2560e6202
Source noteuspto-grants-1984_01