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HRID 16123生成日期:2026年10月23日

海萝胶 → 海萝胶

https://huagongshe.com/zh-CN/reaction/16123

反应方程式

参与物

角色名称HCID投料
反应物海萝胶HCID 313—
反应物NitriteHCID 946—
反应物N,N-二甲基苯胺HCID 949—
反应物N,N-二甲基-2-亚硝基苯胺HCID 21646762—
产物海萝胶HCID 313—
产物4-氨基-N,N-二甲基苯胺HCID 7472—

反应步骤

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.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US07737138B2
来源数据集uspto-grants-2010_06
ORD IDord-3fca965c46274572b8aa89ab91bc72e0
来源说明uspto-grants-2010_06