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HRID 16123作成日:2026年10月26日

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/reaction/16123

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物NitriteHCID 946—
反応物N,N-DimethylanilineHCID 949—
反応物N,N-Dimethyl-2-nitrosoanilineHCID 21646762—
生成物Hydrochloric AcidHCID 313—
生成物N,N-dimethyl-p-phenylenediamineHCID 7472—

反応手順

In step (a), nitrosodimethylaniline is prepared from dimethylaniline by treatment with nitrite (NaNO2) in aqueous acid (HCl) solution. In step (b), the nitroso compound is reduced to form p-aminodimethylaniline in aqueous acid (HCl) solution using zinc dust solution. In steps (c), (d), and (e), the p-aminodimethylaniline is oxidized in aqueous acid solution with another molecule of dimethylaniline, and simultaneously a thiosulfonic acid group is introduced; the ring is then closed using manganese dioxide or copper sulfate. More specifically, a clear neutral solution of p-aminodimethylaniline is acidified (H2SO4), and a non-reducing zinc chloride solution is added (ZnCl2 with Na2Cr2O7). Aluminium thiosulfate (Al2(S2O3)3) and sodium thiosulfate (Na2S2O3) are added. Sodium dichromate (Na2Cr2O7) is added. The mixture is heated and aerated. Dimethylaniline is added. Sodium dichromate (Na2Cr2O7) is added. The mixture is heated, and becomes dark greenish-blue in colour due to the formation of the thiosulfonic acid of Bindschedler green. Manganese dioxide or copper sulfate is added, and the mixture heated, and the dye precipitates from the concentrated zinc chloride solution.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737138B2
出典データセットuspto-grants-2010_06
ORD IDord-3fca965c46274572b8aa89ab91bc72e0
出典メモuspto-grants-2010_06