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HRID 1038662作成日:2026年10月25日

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

https://huagongshe.com/reaction/1038662

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TriethylamineHCID 8471—
反応物3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
溶媒DichloromethaneHCID 6344—
生成物N-(4-Methyl-3-nitrophenyl)-3-(trifluoromethyl)benzamideHCID 11716802—

反応手順

To a solution of 4-methyl-3-nitroaniline (5 g, 32.2 mmol, 1.0 eq.) and triethylamine (5.38 ml, 38.6 mmol, 1.2 eq.) in dichloromethane (100 ml) is added a solution of 3-trifluoromethylbenzoyl chloride 33.8 mmol, 1.05 eq.) within 30 min. The suspension formed is stirred for 1 h at room temperature. Then, the reaction mixture is diluted with dichloromethane (800 ml) and extracted with water (100 ml), 2M aqueous Na2CO3 (100 ml), 2M HCl (100 ml), water (100 ml). The organic layer is dried over Na2SO4, evaporated to a volume of about 100 ml and diluted with hexanes (100 ml). The precipitate is filtered off, washed with hexanes/dichloromethane 1:1 and hexanes. Vacuum drying over night at room temperatures gives light yellow fine needles: HPLC: tR=6.72 min (purity: >99%, gradient A), ESI-MS: 325.2 [MH]+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08552002B2
出典データセットuspto-grants-2013_10
ORD IDord-7f1ca51656ed403d8d5a940cc47138d5
出典メモuspto-grants-2013_10