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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 443752생성일: 2026년 10월 24일

Nitric Acid → 1,7-Dinitroanthraquinone

https://huagongshe.com/ko/reaction/443752

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물9,10-Anthracenedione, 1,2-dinitro-HCID 42596—
생성물1,7-DinitroanthraquinoneHCID 741471.8%

반응 단계

5.00 kg of this dinitroanthraquinone mixture (consisting of 41.2% of 1,5-dinitroanthraquinone, 39.6% of 1,8-dinitroanthraquinone, 8.9% of 1,6-dinitroanthraquinone and 9.5% of 1,7-dinitroanthraquinone) together with 49.04 kg of 97 percent strength by weight nitric acid (molar ratio 45) continuously flow, per hour, onto the fourth tray of a 5-tray rectifying column at about 55° C. 29.65 kg/hour of 99 percent strength by weight nitric acid is taken off at the head of the column at a reflux ratio of reflux/take-off of 0.4. The column is operated under a head pressure of 200 mm Hg, a head temperature of about 50° C. being set up. 19.29 kg/hour of 70 percent strength by weight nitric acid are continuously added to the sump of the column at a temperature of about 70° C. The dinitro-anthraquinone mixture to be crystallised, in which the molar ratio of nitric acid to organic products is 30:1 and the nitric acid concentration is 82 percent by weight (weight ratio 7.7), is removed at the sump of the column at a temperature of about 70° C. 3.8 kg per hour of a dinitroanthraquinone mixture having a composition of 53.2% of 1,5-dinitroanthraquinone, 44.6% of 1,8-dinitroanthraquinone, 0.3% of 1,6-dinitroanthraquinone and 1.8% of 1,7-dinitroanthraquinone is isolated from the mixture thus obtained, by cooling to room temperature (25° to 30° C.), separating off by filtration the solid which has precipitated and then drying it.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04261908
출처 데이터셋uspto-grants-1981_04
ORD IDord-792088b63b134b5d8f48a9e504cad3b3
출처 메모uspto-grants-1981_04