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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16123생성일: 2026년 10월 25일

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/reaction/16123

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물NitriteHCID 946—
반응물N,N-DimethylanilineHCID 949—
반응물N,N-Dimethyl-2-nitrosoanilineHCID 21646762—
생성물Hydrochloric AcidHCID 313—
생성물N,N-dimethyl-p-phenylenediamineHCID 7472—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737138B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3fca965c46274572b8aa89ab91bc72e0
출처 메모uspto-grants-2010_06