돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 647025생성일: 2026년 10월 26일

1-Nitroanthraquinone → 1-Nitroanthraquinone

https://huagongshe.com/reaction/647025

반응식

참여 물질

역할이름HCID투입량
반응물1-NitroanthraquinoneHCID 6704—
반응물9,10-Anthracenedione, 1,2-dinitro-HCID 42596—
반응물2-NitroanthraquinoneHCID 3928593—
생성물1-NitroanthraquinoneHCID 6704—
생성물1-AminoanthraquinoneHCID 6710—

반응 단계

The nitroanthraquinone used was composed of 69.1% of 1-nitroanthraquinone, 0.7% of 2-nitroanthraquinone and 26.8% of dinitroanthraquinone, and the 1-aminoanthraquinone content in the effluent aminoanthraquinone dry cake was 73.6%. The reduction yield from 1-nitroanthraquinone to 1-aminoanthraquinone was 99.7%. The crystals of the aminoanthraquinones obtained in this and following Examples 2-6 are represented by FIG. 2. They had excellent filterability as tested by a rotary vacuum filter or a pressure filter and could be efficiently separated from waste water of reduction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04407756
출처 데이터셋uspto-grants-1983_10
ORD IDord-ee67a3768129408880265cdd2bac9bce
출처 메모uspto-grants-1983_10