HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296342Generated: October 25, 2026
Diethyl Oxalate → 3-Cyano-2-oxotridecanoic acid ethyl ester
https://huagongshe.com/reaction/2296342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Dodecanenitrile | HCID 17092 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Cyano-2-oxotridecanoic acid ethyl ester | HCID 13276240 | — |
Reaction Steps
0.5 Moles of n-undecyl 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-oxotridecanoic acid ethyl ester. Recrystallization from petroleum ether at 30°-60° C. provides pure material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04428959 |
|---|
| Source dataset | uspto-grants-1984_01 |
|---|
| ORD ID | ord-e3d5a5a442f9490e9a1780403e9bfd39 |
|---|
| Source note | uspto-grants-1984_01 |
|---|