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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 4,4,4-trifluorobutyrateHCID 2733273—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product5,5,5-Trifluoro-2-oxopentanoic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669103B2
Source datasetuspto-grants-2014_03
ORD IDord-0ccbf7c4bea24aa0b7e19cdbb0dfc56d
Source noteuspto-grants-2014_03