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HRID 77696作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
反応物DiisopropylethylamineHCID 81531—
反応物3-Iodo-p-toluidineHCID 118889—
溶媒DichloromethaneHCID 6344—
生成物N-(3-iodo-4-methylphenyl)-3-(trifluoromethyl)benzamideHCID 792550692%

反応条件

温度25 °C

反応手順

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).

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-8e1d154a8b984a23affefa947ae0cdfe
出典メモuspto-grants-2014_09