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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282097Generated: October 31, 2026

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

https://huagongshe.com/reaction/2282097

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 numberUS09139836B2
Source datasetuspto-grants-2015_09
ORD IDord-41a17fb7ac914af1b2dc9e255c9a48d6
Source noteuspto-grants-2015_09