Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1-Nitroanthraquinone → 1-Nitroanthraquinone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1-Nitroanthraquinone | HCID 6704 | — |
| 반응물 | 9,10-Anthracenedione, 1,2-dinitro- | HCID 42596 | — |
| 반응물 | 2-Nitroanthraquinone | HCID 3928593 | — |
| 생성물 | 1-Nitroanthraquinone | HCID 6704 | — |
| 생성물 | 1-Aminoanthraquinone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04407756 |
| 출처 데이터셋 | uspto-grants-1983_10 |
| ORD ID | ord-ee67a3768129408880265cdd2bac9bce |
| 출처 메모 | uspto-grants-1983_10 |