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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77723생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/77723

반응식

참여 물질

역할이름HCID투입량
반응물3-(Trifluoromethyl)anilineHCID 7375—
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물3-Iodo-4-methylbenzoic acidHCID 621640—
촉매DimethylformamideHCID 6228—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물3-iodo-4-methyl-N-(3-(trifluoromethyl)phenyl)benzamideHCID 17197569—

반응 조건

온도0 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841318B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4dcd7be8c7164f178f5cc798c710ebad
출처 메모uspto-grants-2014_09