돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 972999생성일: 2026년 10월 24일

Hydroquinone → 1-Aminoanthraquinone

https://huagongshe.com/ko/reaction/972999

반응식

참여 물질

역할이름HCID투입량
반응물HydroquinoneHCID 785—
반응물1-NitroanthraquinoneHCID 6704—
반응물9,10-Anthracenedione, 1,5-dinitro-HCID 6705—
반응물Sodium HydroxideHCID 14798—
반응물1,8-Dinitro-9,10-anthraquinoneHCID 67210—
반응물HCID 178418361HCID 178418361—
촉매HCID 178418390HCID 178418390—
생성물1-AminoanthraquinoneHCID 671097.4%

반응 조건

온도30 °C

반응 단계

A 500 ml. electromagnetically stirred flask was charged with 5.0 g of crude 1-nitroanthraquinone having a purity of 97% and containing 2% of 1,5-dinitroanthraquinone and 1% of 1,8-dinitroanthraquinone as impurities (0.0l92 mole of 1-nitroanthraquinone, and 0.005 mole of all the dinitroanthraquinones), 100 g (0.1 mole) of a 4% aqueous solution of sodium hydroxide and 0.1 g of 5% palladium-carbon. The inside of the flask was purged with hydrogen, and at a reaction temperature of 30° C., they were stirred. In 3 hours, the reaction was stopped with the absorption of 0.08 mole of hydrogen. The amount of hydrogen absorbed was slightly in excess of the sum of the amount of hydrogen required to convert the nitro group to an amino group (0.0606 mole) and the amount of hydrogen required to convert 1-aminoanthraquinone to its hydroquinone derivative (0.0192 mole). The inside of the flask was purged with nitrogen, and the reaction mixture was filtered in an atmosphere of nitrogen to separate the catalyst. The filtrate was oxidized with air at 20° to 30° C. for 2 hours with stirring to afford 4.2 g of 1-aminoanthraquinone in a yield of 97.4% of theory. The product had a purity of 99% as determined by infrared absorption spectroscopy.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04054586
출처 데이터셋uspto-grants-1977_10
ORD IDord-9bc872d6daec4f4a807b833faff29f5d
출처 메모uspto-grants-1977_10