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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407201Generated: October 30, 2026

Diethyl Oxalate → 5,5,5-Trifluoro-2-oxopentanoic acid

https://huagongshe.com/reaction/2407201

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 numberUS08809529B2
Source datasetuspto-grants-2014_08
ORD IDord-2358ddc2129b4bbe9e20abdd1871e970
Source noteuspto-grants-2014_08