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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 556196생성일: 2026년 10월 25일

Sodium Hydroxide → 1,8-Diamino-9,10-anthracenedione

https://huagongshe.com/reaction/556196

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물1,8-Dinitro-9,10-anthraquinoneHCID 67210—
반응물Sodium sulfide nonahydrateHCID 73972—
반응물1,8-Bis(chloroacetamido)anthraquinoneHCID 46928041—
용매EthanolHCID 702—
생성물1,8-Diamino-9,10-anthracenedioneHCID 8511—

반응 단계

In the step S1, a manufacturing method of 1,8-bis(chloroacetamido)anthraquinone includes the steps of: add 1,8-dinitroanthraquinone with ethanol, and then add sodium sulfide nonahydrate and sodium hydroxide solution into the mixture to be mixed and reflux heated. After standing and filtration, 1,8-diaminoanthraquinone is obtained by recrystallization of the solution. Next the 1,8-diaminoanthraquinone is dissolved in N,N-dimethylform amide, and pyridine is added for catalyzing, and then chloroacetyl chloride is added into and mixed with the mixture to react. Pour the solution into ice water, 1,8-bis(chloroacetamido) anthraquinone is obtained after filtration and recrystallization of the solution. The step of adding pyridine for catalyzing is run under an ice-bath while in the step of adding and mixing chloroacetyl chloride into the mixture, the ice bath is removed, the nitrogen gas is introduce and the step is run under light protection condition. The step of adding and mixing chloroacetyl chloride into the mixture is run at the room temperature for 24 hours.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08053583B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-41fb87150f0247df9b854dce5420b4c7
출처 메모uspto-grants-2011_11