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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233673생성일: 2026년 10월 25일

Piperonal → 3,4-Methylenedioxybenzylidenesuccinic acid

https://huagongshe.com/reaction/233673

반응식

참여 물질

역할이름HCID투입량
반응물PiperonalHCID 8438—
반응물Diethyl SuccinateHCID 31249—
반응물SodiumHCID 5360545—
용매EthanolHCID 702—
생성물3,4-Methylenedioxybenzylidenesuccinic acidHCID 243789—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05594006
출처 데이터셋uspto-grants-1997_01
ORD IDord-2c2c1f3c36c045219cd3364ec6cc4970
출처 메모uspto-grants-1997_01