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HRID 17063作成日:2026年10月25日

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

https://huagongshe.com/reaction/17063

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US07737295B2
出典データセットuspto-grants-2010_06
ORD IDord-af5aad6c0b7141c09bdc994dbba30573
出典メモuspto-grants-2010_06