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HRID 1858874作成日:2026年10月27日

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

https://huagongshe.com/reaction/1858874

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-DimethylanilineHCID 7949—
反応物Disperse orange 3HCID 12896—
反応物Sodium HydroxideHCID 14798—
反応物Sodium AcetateHCID 517045—
反応物Sodium NitriteHCID 23668193—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物4-[4'-(4"-Nitrophenylazo)phenylazo]-3,5-dimethylanilineHCID 5439382161%

反応条件

温度5 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06153272
出典データセットuspto-grants-2000_11
ORD IDord-f4627ddeb8094052b45573f08384758d
出典メモuspto-grants-2000_11