参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 海萝胶 | HCID 313 | — |
| 反应物 | Nitrite | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07737138B2 |
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| 来源数据集 | uspto-grants-2010_06 |
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| ORD ID | ord-3fca965c46274572b8aa89ab91bc72e0 |
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| 来源说明 | uspto-grants-2010_06 |
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