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HRID 77723作成日:2026年10月25日

3-(Trifluoromethyl)aniline → 3-iodo-4-methyl-N-(3-(trifluoromethyl)phenyl)benzamide

https://huagongshe.com/reaction/77723

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Trifluoromethyl)anilineHCID 7375—
反応物Oxalyl chlorideHCID 65578—
反応物DiisopropylethylamineHCID 81531—
反応物3-Iodo-4-methylbenzoic acidHCID 621640—
触媒DimethylformamideHCID 6228—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物3-iodo-4-methyl-N-(3-(trifluoromethyl)phenyl)benzamideHCID 17197569—

反応条件

温度0 °C

反応手順

To a suspension of 3-iodo-4-methylbenzoic acid (3.00 g, 11.4 mmol) in DCM (30 mL) at 0° C. was added oxalyl chloride (1.45 mL, 17.2 mmol) followed by two drops of DMF. The reaction was stirred at 0° C. for 30 minutes followed by warming to ambient temperature for 40 minutes. The mixture was concentrated in vacuo. To the resulting residue was added DCM (30 mL), DIPEA (2.99 mL, 17.2 mmol) and 3-(trifluoromethyl)-benzenamine (1.42 mL, 11.4 mmol). The reaction was stirred at ambient temperature for 1 hour. The mixture was then poured into water, and the product was extracted with DCM. The combined organic extracts were washed with water, followed by saturated sodium bicarbonate, and then dried over sodium sulfate. An equal volume of hexane was added and most of the DCM was then removed in vacuo. The resulting yellow solid was filtered, rinsed with hexane and air dried. (4.27 g, 92%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841318B2
出典データセットuspto-grants-2014_09
ORD IDord-4dcd7be8c7164f178f5cc798c710ebad
出典メモuspto-grants-2014_09