HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398987Generated: October 25, 2026
Diethyl Oxalate → Diethyl 2-butyl-3-oxobutanedioate
https://huagongshe.com/reaction/398987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Ethyl hexanoate | HCID 31265 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Diethyl 2-butyl-3-oxobutanedioate | HCID 251159 | — |
Reaction Steps
100 ml of ether, then 13.55 ml of diethyl oxalate were added to a solution of sodium ethylate prepared by stirring 2.3 g of sodium and 150 ml of ethanol at 40° C. for one hour. The mixture was refluxed for 15 minutes, cooled down slightly and 50 ml of ethyl caproate were added. The mixture was stirred at reflux for 3 hours and at 30° C. to 35° C. for 16 hours. 50 ml of water were added and the aqueous phase was separated by decanting, washed twice with ether and acidified with 2N hydrochloric acid. Extraction was carried out 3 times with ether and the combined organic phases were washed with water, then with a saturated solution of sodium chloride, dried and evaporated to dryness to obtain 9.5 g of the desired product which was used as is for the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05817674 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-88d0b947f0114e4dae17c9002676060a |
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| Source note | uspto-grants-1998_10 |
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