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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1038662생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1038662

반응식

참여 물질

역할이름HCID투입량
반응물4-Methyl-3-nitroanilineHCID 8390—
반응물TriethylamineHCID 8471—
반응물3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
용매DichloromethaneHCID 6344—
생성물N-(4-Methyl-3-nitrophenyl)-3-(trifluoromethyl)benzamideHCID 11716802—

반응 단계

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]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08552002B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-7f1ca51656ed403d8d5a940cc47138d5
출처 메모uspto-grants-2013_10