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HRID 967890作成日:2026年10月27日

4-Methyl-3-nitroaniline → N-(4-Methyl-3-nitrophenyl)-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/967890

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methyl-3-nitroanilineHCID 8390—
反応物3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
溶媒PyridineHCID 1049—
生成物N-(4-Methyl-3-nitrophenyl)-3-(trifluoromethyl)benzamideHCID 11716802—

反応条件

温度80 °C

反応手順

A mixture of 3-trifluoromethylbenzoyl chloride (9.9 ml), 3-nitro-4-methylaniline (10 g) and pyridine (100 ml) was stirred and heated to 80° C. for 2 hours. The reaction mixture was evaporated and the residue was triturated under 2N aqueous hydrochloric acid solution. The solid so obtained was isolated, washed in turn with a saturated aqueous sodium bicarbonate solution, water and isohexane and dried under vacuum at 55° C. to give N-(4-methyl-3-nitrophenyl)-3-trifluoromethylbenzamide as a solid (21.9 g); NMR Spectrum: (DMSOd6) 7.49 (d, 1H), 7.78 (m, 1H), 7.99 (m, 2H), 8.27 (m, 2H), 8.51 (s, 1H), 10.77 (s, 1H); Mass Spectrum: M−H− 23.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06956037B2
出典データセットuspto-grants-2005_10
ORD IDord-ebeb4a8f63ed4958bd3863cb65cadbbb
出典メモuspto-grants-2005_10