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HRID 1719639생성일: 2026년 10월 24일

1-Chloro-2,4-Dinitrobenzene → 6-Methoxy-3-acetylamino-aniline hydrochloride

https://huagongshe.com/ko/reaction/1719639

반응식

참여 물질

역할이름HCID투입량
반응물1-Chloro-2,4-DinitrobenzeneHCID 6—
반응물Hydrochloric AcidHCID 313—
반응물Acetic AnhydrideHCID 7918—
반응물2,4-DiaminoanisoleHCID 11976—
반응물Sodium HydroxideHCID 14798—
반응물3'-Amino-4'-methoxyacetanilideHCID 80779—
반응물Acetamide, N,N'-(4-methoxy-1,3-phenylene)bis-HCID 153420—
반응물Magnesium monoxideHCID 6850729—
용매MethanolHCID 887—
생성물6-Methoxy-3-acetylamino-aniline hydrochlorideHCID 20267377100%

반응 단계

197 parts of 37% strength hydrochloric acid are added dropwise, at 20°-25° C. in the course of 30 minutes, with stirring, to a dark solution, obtained according to Example 1 of European Pat. No. 0,011,048 by reaction of 213 parts of 2,4-dinitrochlorobenzene with 42 parts of sodium hydroxide in 632 parts of methanol, subsequent hydrogenation on Pd/charcoal at 60° C. and then acetylation with 98 parts of acetic anhydride in the presence of 22 parts of magnesium oxide at 0°-5° C., of 6-methoxy-3-acetylamino-aniline which, according to "high performance liquid chromatography analysis" ("HPLC analysis") contains 8.9 parts of 2,4-bis-acetylaminoanisole and 3.5 parts of 2,4-diaminoanisole, as well as black decomposition products formed by oxidation, in addition to 153 parts of the target product. The mixture is subsequently stirred for 1 hour and cooled to 0°-5° C. and the 6-methoxy-3-acetylamino-aniline hydrochloride precipitated is isolated by filtration. The product is washed twice with 100 parts of methanol to give, after drying in vacuo, 188.5 parts of 6-methoxy-3-acetylamino-aniline hydrochloride, which, besides about 5% of magnesium chloride, contains no organic by-products detectable by thin-layer chromatography ("TLC") or HPLC analysis. The product isolated thus corresponds to 179.1 parts of 100% pure 6-methoxy-3-acetylamino-aniline hydrochloride, which corresponds to a yield of 82.7% of theory, based on the 2,4-dinitrochlorobenzene employed.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04540815
출처 데이터셋uspto-grants-1985_09
ORD IDord-30c2f68fe11b431ebc8eb3b1a6e331f1
출처 메모uspto-grants-1985_09