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HRID 647025作成日:2026年10月27日

1-Nitroanthraquinone → 1-Nitroanthraquinone

https://huagongshe.com/reaction/647025

反応式

関与物質

役割名称HCID仕込み量
反応物1-NitroanthraquinoneHCID 6704—
反応物9,10-Anthracenedione, 1,2-dinitro-HCID 42596—
反応物2-NitroanthraquinoneHCID 3928593—
生成物1-NitroanthraquinoneHCID 6704—
生成物1-AminoanthraquinoneHCID 6710—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04407756
出典データセットuspto-grants-1983_10
ORD IDord-ee67a3768129408880265cdd2bac9bce
出典メモuspto-grants-1983_10