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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616847Generated: November 1, 2026

Acetone → 2,4-Pentanedione, 1-phenyl-

https://huagongshe.com/reaction/1616847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl phenylacetateHCID 7590—
SolventDiethyl EtherHCID 3283—
Product2,4-Pentanedione, 1-phenyl-HCID 1872369.3%

Reaction Steps

To a solution of NaNH2 (19.02 g, 480 mmol) in anhydrous ether (400 mL) under N2 at −5° C. was added dropwise ethyl phenylacetate (19.2 g, 150 mmol) and then acetone (21.23 g, 370 mmol) with vigorous stirring. After addition, the reaction mixture was stirred at room temperature overnight. The mixture was then acidified to pH 4.0-5.0 with 1 N HCl. The organic layer was separated and concentrated in vacuo. The crude product was purified by silica gel chromatography to give 1-phenyl-2,4-pentanedione (18.32 g, 44%). 1H NMR (400 MHz, CDCl3-d3) δ 15.49 (br s, 1H), 7.33-7.45 (m, 5H), 5.53 (s, 1H), 3.66 (s, 2H), 2.10 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765792B2
Source datasetuspto-grants-2014_07
ORD IDord-cfe46e24b7ad48059ef923a5af950bd5
Source noteuspto-grants-2014_07