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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 973000생성일: 2026년 10월 26일

Hydroquinone → 1-Aminoanthraquinone

https://huagongshe.com/reaction/973000

반응식

참여 물질

역할이름HCID투입량
반응물HydroquinoneHCID 785—
반응물1-NitroanthraquinoneHCID 6704—
반응물9,10-Anthracenedione, 1,5-dinitro-HCID 6705—
반응물AnthraquinoneHCID 6780—
반응물1,8-Dinitro-9,10-anthraquinoneHCID 67210—
반응물2-NitroanthraquinoneHCID 3928593—
반응물HCID 178418361HCID 178418361—
생성물1-AminoanthraquinoneHCID 671072.6%

반응 단계

5.0 g of crude 1-nitroanthraquinone containing dinitroanthraquinones having a purity of 81% and containing 8% of 1,5-dinitroanthraquinone, 4% of 1,8-dinitroanthraquinone and 7% of other dinitroanthraquinones and being free from anthraquinone and 2-nitroanthraquinone (0.016 mole of 1-nitroanthraquinone and 0.0032 mold of all the dinitroanthraquinones) was hydrogenated in the same way as in Example 5. The reaction was stopped when the amount of hydrogen absorbed reached 0.0816 mole, and the inside of the flask was purged with nitrogen. The amount of hydrogen absorbed corresponded to the sum of the amount of hydrogen required to convert the nitro group to an amino group (0.0672 mole) and 90% of the amount of hydrogen required to convert 1-aminoanthraquinone to its hydroquinone derivative (0.0144 mole). The reaction mixture was filtered in a stream of nitrogen to separate the catalyst and insoluble materials from it. The filtrate was oxidized with air at 20° to 30° C. for 2 hours with stirring to afford 3.2 g of 1-aminoanthraquinone having a purity of 98%. The yield of the product was 88% on a purity basis. The resulting 1-aminoanthraquinone contained about 1% of 1,8-diaminoanthraquinone and only traces of other diamino isomers.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04054586
출처 데이터셋uspto-grants-1977_10
ORD IDord-967d535ca9b3419b8022045db011473e
출처 메모uspto-grants-1977_10