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HRID 217506作成日:2026年10月26日

Iodine → 1-Iodo-3-methoxy-5-(trifluoromethyl)benzene

https://huagongshe.com/reaction/217506

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Tert-Butyl nitriteHCID 10906—
反応物5-(Trifluoromethyl)-m-anisidineHCID 605671—
反応物Sodium BisulfiteHCID 23665763—
溶媒ChloroformHCID 6212—
生成物1-Iodo-3-methoxy-5-(trifluoromethyl)benzeneHCID 19773106—

反応条件

温度50 °C

反応手順

3-methoxy-5-(trifluoromethyl)aniline (100 mg, 0.52 mmol) was dissolved in CHCl3 (5.2 mL) and t-butyl nitrite (124 μL, 1.05 mmol) was added dropwise by syringe. Iodine (266 mg, 1.05 mmol) was added and then the reaction was slowly heated to 50° C. and was maintained at this temperature for an hour and thirty minutes. The reaction was then cooled to room temperature and poured into aq. NaHSO3 (50 mL). The mixture was extracted with EtOAc (50 mL) and the organic extracts were washed with aq. NaHSO3 (3×50 mL) and brine (20 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 1% to 15% EtOAc/hexanes afforded 1-iodo-3-methoxy-5-(trifluoromethyl)benzene. Rf=0.75 (25% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 7.53 (s, 1H), 7.41 (s, 1H), 7.09 (s, 1H), 3.82 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193365B2
出典データセットuspto-grants-2012_06
ORD IDord-c321e336100044fd94451ca9baf8a52b
出典メモuspto-grants-2012_06