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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 904626생성일: 2026년 10월 26일

6-Nitro-1,3-benzodioxole-5-carboxaldehyde → 6-Nitro-1,3-benzodioxole-5-carboxylic acid

https://huagongshe.com/reaction/904626

반응식

참여 물질

역할이름HCID투입량
반응물6-Nitro-1,3-benzodioxole-5-carboxaldehydeHCID 12840—
반응물Potassium HydroxideHCID 14797—
반응물Potassium PermanganateHCID 516875—
용매WaterHCID 962—
생성물6-Nitro-1,3-benzodioxole-5-carboxylic acidHCID 246435—

반응 단계

To a slurry of 78 g of 4,5-methylenedioxy-2-nitrobenzaldehyde and 1.5 liter of water there was added a solution of 90 g of potassium permanganate in 1.5 liter of water over a period of 45 minutes. The mixture was then stirred at 70°-80° C. for an additional hour and then made alkaline with 400 ml of aqueous 10% potassium hydroxide. The mixture was filtered while hot to remove the precipitate which was washed with 2 portions of hot water. The filtrate was cooled for 16 hours and the solid which formed was separated by filtration to give recovered starting material. The new filtrate was acidified with concentrated hydrochloric acid and allowed to stand for 3 hours. The yellow solid which formed was separated by filtration to give crude product. The filtrate obtained was extracted with 4 portions of ethyl acetate and the combined extracts were dried over sodium sulfate and added to a solution of the previously obtained crude product in ethyl acetate. The ethyl acetate solution was concentrated, the resulting solid was slurried with chloroform, separated by filtration and dried to give 4,5-methylenedioxy-2-nitrobenzoic acid melting at about 160°-163° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04419357
출처 데이터셋uspto-grants-1983_12
ORD IDord-14600f6875dc40ada72bd384a19413db
출처 메모uspto-grants-1983_12