Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611897Generated: October 26, 2026

Ethyl benzoylacetate → 4-Penten-1-one, 1-phenyl-

https://huagongshe.com/reaction/1611897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl benzoylacetateHCID 7170—
ReactantAllyl bromideHCID 7841—
ReactantPotassium HydroxideHCID 14797—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-Penten-1-one, 1-phenyl-HCID 10136298%
ProductSodiumHCID 5360545—

Reaction Steps

A sodium solution of alcohol was prepared by dissolving 33 g of sodium in 1000 mL of ethanol. To the warm solution, 260 mL of benzoyl-acetic acid-ethylester was added and then 130 mL of allyl bromide was slowly dropped into the solution. The mixture was refluxed for 4 hrs. and then the solid removed in a vacuum. The resulting solid was then combined in an aqueous solution of potassium hydroxide prepared by combining 145 g of potassium hydroxide with 500 mL of water. This mixture was heated under reflux for 4 hrs. The mixture was then neutralized and extracted three times with 150 mL of diethylether. The organic layer was separated, washed twice with water, and dried. The solvent was removed in a vacuum to produce a 98 percent yield of phenyl-(but-3-enyl) ketone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06992035B2
Source datasetuspto-grants-2006_01
ORD IDord-b497c97bcb2341b6b6c9000bad0bb20b
Source noteuspto-grants-2006_01