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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1858874생성일: 2026년 10월 26일

3,5-Dimethylaniline → 4-[4'-(4"-Nitrophenylazo)phenylazo]-3,5-dimethylaniline

https://huagongshe.com/reaction/1858874

반응식

참여 물질

역할이름HCID투입량
반응물3,5-DimethylanilineHCID 7949—
반응물Disperse orange 3HCID 12896—
반응물Sodium HydroxideHCID 14798—
반응물Sodium AcetateHCID 517045—
반응물Sodium NitriteHCID 23668193—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물4-[4'-(4"-Nitrophenylazo)phenylazo]-3,5-dimethylanilineHCID 5439382161%

반응 조건

온도5 °C

반응 단계

A 4 g (16.53 mmol) amount of 4-amino-4'-nitroazobenzene (Disperse Orange 3) was dissolved in ice-cooled acetic acid (100 mL) containing 8 mL of 98% sulfuriic acid. Sodium nitrite (1.48 g, 21.40 mmol) dissolved in a small amount of water (less than 2 mL) was added dropwise to the stirred solution. The reaction temperature was maintained at 5° C. After 6 h of stirring, 3,5-dimethylaniline (5.0 g, 41.30 mmol) in 10 mL of acetic acid was added followed by slow addition of sodium acetate (4.10 g, 50.0 mmol). The resulting red solution was stirred at 5° C. for an additional 16 h. A 10% sodium hydroxide solution was slowly added to neutralize the reaction mixture. The precipitates formed were collected by filtration, washed with water several times, dissolved in THF, and dried over magnesium sulfate. Solvent was evaporated, and a dark red powder was obtained by precipitation in n-hexane. The solid was further purified by column chromatography (silica gel; THF: n-hexane=4 6), affording 3.51 g (61%) of 4-[4'-(4"-nitrophenylazo)phenylazo]-3,5-dimethylaniline as a dark red solid product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06153272
출처 데이터셋uspto-grants-2000_11
ORD IDord-f4627ddeb8094052b45573f08384758d
출처 메모uspto-grants-2000_11