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HRID 32944作成日:2026年10月25日

Methanol → 4-Amino-5-iodo-2-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/32944

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物N-IodosuccinimideHCID 120273—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物4-Amino-2-(trifluoromethyl)benzonitrileHCID 522170—
溶媒TetrahydrofuranHCID 8028—
溶媒AluminumHCID 5359268—
生成物4-Amino-5-iodo-2-(trifluoromethyl)benzonitrileHCID 25067377—

反応手順

4-Amino-2-trifluoromethyl-benzonitrile (20.44 g, 109.79 mmoles) and p-toluenesulfonic acid monohydrate (1.05 g, 5.52 mmoles) were dissolved methanol (200 mL) and THF (200 mL), and the reaction mixture was stirred under a nitrogen atmosphere. The reaction vessel was wrapped in aluminium foil, while the solution was stirred for 20 min., then N-iodosuccinimide (30.41 g, 135.17 mmoles) was added and the reaction was allowed to stir overnight (16 hrs). The reaction mixture was concentrated in vacuo, triturated with hexanes (3×400 mL) and concentrated to dryness. The crude solid was dissolved in diethyl ether (400 mL), washed with water (3×), the organic extracts were diluted with hexanes (400 mL) and a white solid precipitated. The solid was filtered and dried in a vacuum oven (35° C. @762 Torr) overnight to yield the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427682B2
出典データセットuspto-grants-2008_09
ORD IDord-1fd312ac805b4dfeadac16093750d1c8
出典メモuspto-grants-2008_09