HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184325Generated: October 27, 2026
Diethyl Oxalate → 5,5,5-Trifluoro-2-oxopentanoic acid
https://huagongshe.com/reaction/1184325
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 4,4,4-trifluorobutyrate | HCID 2733273 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5,5,5-Trifluoro-2-oxopentanoic acid | HCID 14278600 | — |
Reaction Steps
Ethyl 4,4,4-trifluorobutyrate (1 g, 5.88 mmol) and diethyl oxalate (3.87 g, 26.5 mmol) was dissolved in ethanol. Sodium ethoxide (21% in ethanol, 2.09 g) was added to the solution, and the reaction mixture stirred for 0.5 hrs. Solvent was distilled, and the residue extracted with EtOAc/water. The organic layers were collected and dried over sodium sulfate. After filtration, solvent was removed to give a clear liquid. MS (ESI): m/z 269.1 (M−1). The liquid was then dissolved in 3N HCl (20 mL), and the reaction mixture refluxed for 4 hrs. After cooling down, the reaction mixture was extracted with EtOAc. The organic layers were collected and dried over sodium sulfate. After filtration, solvent was removed, and the residue used directly in the next step. MS (ESI): m/z 169.7 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08669103B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-0ccbf7c4bea24aa0b7e19cdbb0dfc56d |
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| Source note | uspto-grants-2014_03 |
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