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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620808Generated: October 29, 2026

Water → 3-Acetyl-5-Ethyldihydro-2(3H)-Furanone

https://huagongshe.com/reaction/620808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,2-EpoxybutaneHCID 7834—
ReactantEthyl AcetoacetateHCID 8868—
ReactantSodium HydroxideHCID 14798—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product3-Acetyl-5-Ethyldihydro-2(3H)-FuranoneHCID 1105189745%

Reaction Steps

2-acetyl-4-ethyl butyrolactone was prepared from ethylacetoacetate and 1,2-epoxybutane according to the method described in Johnson U.S. Pat. No. 2,443,827. A mixture of 40 g sodium hydroxide (1.0 mole), 270 ml water and 90 ml ethanol was cooled to 0°, stirred, and 130 g ethylacetoacetate (1.0 mole) and 72 g 1,2-epoxybutane (1.0 mole) added. Stirring was continued at 0°, and the mixture was thereafter left at 4° C. for 48 hours. The reaction mixture was neutralized with 80 ml acetic acid, extracted with toluene, washed with water, sodium bicarbonate and finally with water. The mixture was then dried (magnesium sulfate), filtered and the solvent removed, leaving a product, bp 86°-96°-/0.1 mm, in 45% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04822813
Source datasetuspto-grants-1989_04
ORD IDord-d292a9983997441cbb60be08acd78418
Source noteuspto-grants-1989_04