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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534088Generated: October 27, 2026

Benzoic Acid → 3-(Benzoyloxy)-2,4-pentanedione

https://huagongshe.com/reaction/534088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantDimethylformamideHCID 6228—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Chloro-2,4-pentanedioneHCID 74328—
SolventWaterHCID 962—
Product3-(Benzoyloxy)-2,4-pentanedioneHCID 2073896.12%

Reaction Conditions

Temperature50 °C

Reaction Steps

A flask was charged with powdered potassium hydroxide (21.89 g, 390.2 mmol), benzoic acid (47.65 g, 390.2 mmol), and DMF (500 mL) was added. The mixture was heated at 50° C. for 1 hour. 3-Chloropentane-2,4-dione (52.5 g, 390.2 mmol) was added and the reaction was stirred at 50° C. overnight. The reaction was cooled to ambient temperature, diluted in water (1.5 L) and extracted with ether (3×500 mL). The combined organic layers were washed with water, saturated NH4Cl and brine. The organic layer was dried over sodium sulfate and concentrated in vacuo to afford 2,4-dioxopentan-3-yl benzoate (82.59 g, 96.12% yield) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853409B2
Source datasetuspto-grants-2014_10
ORD IDord-80a427b546934ca1b4d36365787bb86f
Source noteuspto-grants-2014_10