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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77696생성일: 2026년 10월 24일

3-(Trifluoromethyl)benzoyl chloride → N-(3-iodo-4-methylphenyl)-3-(trifluoromethyl)benzamide

https://huagongshe.com/ko/reaction/77696

반응식

참여 물질

역할이름HCID투입량
반응물3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
반응물DiisopropylethylamineHCID 81531—
반응물3-Iodo-p-toluidineHCID 118889—
용매DichloromethaneHCID 6344—
생성물N-(3-iodo-4-methylphenyl)-3-(trifluoromethyl)benzamideHCID 792550692%

반응 조건

온도25 °C

반응 단계

To 3-iodo-4-methylaniline (500.0 mg, 2.145 mmol) was added dichloromethane (DCM) (10 mL) followed by N,N-diisopropylethylamine (DIPEA)(520 μL, 3.0 mmol) and 3-(trifluoromethyl)-benzoyl chloride (0.36 mL, 2.4 mmol). The reaction was stirred at 25° C. for 16 hours and was transferred to a separatory funnel and partitioned between water and dichloromethane (DCM). The organic phase was sequentially washed with 0.1N HCl, saturated aqueous NaHCO3, water, then saturated aqueous NaCl. The washed organic phase was then dried over MgSO4 and filtered and concentrated to leave the crude product. The crude product was triturated with hexanes to leave the product as an off-white solid, (797 mg, 92%). 1H NMR (400 MHz, CDCl3): δ 8.10 (m, 2H), 8.04 (d, 1H), 7.84 (bs, 1H), 7.81 (d, 1H), 7.63 (m, 1H), 7.58 (dd, 1H), 7.22 (d, 1H), 2.42 (s, 3H). MS (EI) m/z=274 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841318B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-8e1d154a8b984a23affefa947ae0cdfe
출처 메모uspto-grants-2014_09