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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 441768생성일: 2026년 10월 26일

Dimethylformamide → 2,3-Anthracenedicarbonitrile, 1,4-diamino-9,10-dihydro-9,10-dioxo-

https://huagongshe.com/reaction/441768

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium CyanideHCID 8929—
반응물Ammonium ChlorideHCID 25517—
반응물Disperse Violet 28HCID 65731—
생성물2,3-Anthracenedicarbonitrile, 1,4-diamino-9,10-dihydro-9,10-dioxo-HCID 66477—

반응 조건

온도120 °C

반응 단계

31 parts of 1,4-diamino-2,3-dichloroanthraquinone is introduced into 280 parts by volume of dimethylformamide and the whole is heated to 120° C. At this temperature 30 parts of sodium cyanide is introduced in about five minutes, the supply of heat being decreased because the temperature is maintained by the heat of reaction. After a short time the exothermic reaction ceases and the whole is heated at 125° to 130° C. for about another 35 minutes. After this period the whole of the starting material has reacted. The whole is cooled to 110° C., 11 parts of ammonium chloride is added and the solvent is substantially distilled off at subatmospheric pressure; 200 to 210 parts by volume of dimethylformamide is recovered. The residue in the still is stirred vigorously while 300 parts of water is slowly added; the reaction product is thus precipitated. The whole is stirred for about another hour until the product has become easily filterable, and suction filtered while hot, and the filter cake is washed with hot water until the water running away has become colorless. The product is rinsed with methanol and dried. 26 parts of 1,4-diaminoanthraquinone-2,3-dinitrile is obtained. The product has the same properties as those obtained according to Examples 1 and 2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04042605
출처 데이터셋uspto-grants-1977_08
ORD IDord-01a05c2f560a45339bb229a1ed19861b
출처 메모uspto-grants-1977_08