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HRID 1635589作成日:2026年10月26日

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

https://huagongshe.com/reaction/1635589

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl benzoylacetateHCID 7170—
反応物Allyl bromideHCID 7841—
反応物Potassium HydroxideHCID 14797—
反応物SodiumHCID 5360545—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物4-Penten-1-one, 1-phenyl-HCID 10136298%
生成物SodiumHCID 5360545—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06509427B1
出典データセットuspto-grants-2003_01
ORD IDord-41546d020d7d4f4798a1cf6bd547e613
出典メモuspto-grants-2003_01