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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32944생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/32944

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물N-IodosuccinimideHCID 120273—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물4-Amino-2-(trifluoromethyl)benzonitrileHCID 522170—
용매TetrahydrofuranHCID 8028—
용매AluminumHCID 5359268—
생성물4-Amino-5-iodo-2-(trifluoromethyl)benzonitrileHCID 25067377—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427682B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-1fd312ac805b4dfeadac16093750d1c8
출처 메모uspto-grants-2008_09