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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261902생성일: 2026년 10월 25일

N,N-Diethylaniline → 4-Chloro-3,5-dinitrotoluene

https://huagongshe.com/reaction/261902

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DiethylanilineHCID 7061—
반응물Calcium CarbonateHCID 10112—
반응물2,6-Dinitro-p-cresolHCID 11872—
반응물Phosphorus oxychlorideHCID 24813—
생성물4-Chloro-3,5-dinitrotolueneHCID 78918—

반응 조건

온도90 °C

반응 단계

About 100 parts (0.43 mol) of 4-hydroxy-3,5-dinitrotoluene, about 750 parts by volume of phosphorus oxychloride and about 1250 parts by volume of diethylaniline which has been dried over calcium carbonate are heated together to about 90° C. for about 21/2 hours with stirring. The reaction mixture is poured onto ice and extracted with methylene chloride, and the methylene chloride is removed in a rotary evaporator. After recrystallization from ethanol, about 65 parts of 4-chloro-3,5-dinitrotoluene of melting point of about 112° C. to about 113° C. about 70% of the theoretical yield is obtained. About 52 parts (0.24 mol) of this isolated compound are dissolved in about 500 parts by volume of toluene and added dropwise to a boiling mixture of about 180 parts of deoiled iron into about 180 parts by volume of H2O, about 280 parts by volume of toluene and about 5 parts by volume of glacial acetic acid. After about 3 hours, the reaction mixture is removed from the iron by suction filtration and then extracted with boiling toluene. The water is removed in a separating funnel and the organic phase is removed under vacuum. About 34 parts (91% of theoretical) of 4-chloro-3,5-diaminotoluene, melting point about 116° C. are obtained as white needles from 1:1 benzene/cyclohexane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04152510
출처 데이터셋uspto-grants-1979_05
ORD IDord-cc08456cdf104a979bc0b1b35080a898
출처 메모uspto-grants-1979_05