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HRID 37537作成日:2026年10月24日

Hydrochloric Acid → (5S)-5-phenyloxolan-2-one

https://huagongshe.com/ja/reaction/37537

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium HydroxideHCID 14798—
反応物3-Benzoylpropionic acidHCID 72871—
反応物HCID 178418361HCID 178418361—
溶媒EthanolHCID 702—
生成物(5S)-5-phenyloxolan-2-oneHCID 695022463%

反応条件

温度40 °C

反応手順

In a 100 ml autoclave were charged 1.78 g (10 mmole) of 4-phenyl-4oxobutyric acid and 14 ml of ethanol. A solution separately prepared from 44.9 mg (0.05 mmole) of ##STR13## double the molar quantity of concentrated hydrochloric acid, and 5 ml of ethanol was added to the above-prepared solution in a nitrogen atmosphere to conduct hydrogenation at 35° C. and at a hydrogen pressure of 70 kg/cm2 for 230 hours. To the reaction mixture was added 8 ml of a 10% sodium hydroxide aqueous solution, followed by stirring at 40° C. for 3 hours. After cooling to room temperature, the resulting solution was extracted twice with 30 ml portions of methylene chloride. The organic layer was removed, and the aqueous layer was adjusted to a pH of 4 with a 10% hydrochloric acid aqueous solution and then again extracted thrice with 20 ml portions of methylene chloride. The combined extract was concentrated, and the residue was purified by silica gel column chromatography using hexanediethyl ether as a developing solvent to obtain 1.02 g (percent yield: 63%) of (S)-4-phenyl-γ-butyrolactone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420306
出典データセットuspto-grants-1995_05
ORD IDord-cff20513efce4e30ac8b198e75cc2c68
出典メモuspto-grants-1995_05