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HRID 233673作成日:2026年10月26日

Piperonal → 3,4-Methylenedioxybenzylidenesuccinic acid

https://huagongshe.com/reaction/233673

反応式

関与物質

役割名称HCID仕込み量
反応物PiperonalHCID 8438—
反応物Diethyl SuccinateHCID 31249—
反応物SodiumHCID 5360545—
溶媒EthanolHCID 702—
生成物3,4-Methylenedioxybenzylidenesuccinic acidHCID 243789—

反応手順

Dissolving 19.14 g of metal sodium in 400 ml of ethanol, 110.8 ml of diethyl succinate and 100 g of piperonal were added, and the solution was heated and refluxed for 3 hours. The reaction solution was concentrated in vacuo, and the residue was dissolved in 700 ml of water, and washed with 300 ml of diethyl ether. The water layer was stirred in ice, adjusted to pH 1 by concentrated hydrochloric acid, and extracted with 300 ml of diethyl ether. The diethyl ether layer was washed once with saturated brine, and dried over magnesium sulfate anhydride, and concentrated in vacuo. The obtained oily residue was dissolved by 181.4 g in 350 ml of ethanol, and 400 ml of 5N sodium hydroxide was added to stir overnight at room temperature. The reaction solution was concentrated in vacuo, and the residue was washed with 200 ml of diethyl ether. The water layer was stirred in ice, adjusted to pH 1 by concentrated hydrochloric acid, and extracted with 400 ml of ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over magnesium sulfate anhydride, and concentrated in vacuo. To the obtained residue, 300 ml of diethyl ether was added to solidify, and the captioned compound was obtained. Yield: 67.34 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05594006
出典データセットuspto-grants-1997_01
ORD IDord-2c2c1f3c36c045219cd3364ec6cc4970
出典メモuspto-grants-1997_01