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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32927생성일: 2026년 10월 24일

Methanol → 2-Iodo-4-nitro-5-(trifluoromethyl)aniline

https://huagongshe.com/ko/reaction/32927

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물p-Toluenesulfonic acidHCID 6101—
반응물4-Nitro-3-(trifluoromethyl)anilineHCID 94955—
반응물N-IodosuccinimideHCID 120273—
용매TetrahydrofuranHCID 8028—
생성물2-Iodo-4-nitro-5-(trifluoromethyl)anilineHCID 45588271—

반응 단계

5-Amino-2-nitrobenzotrifluoride (16.25 g, 78.8 mmol) was dissolved in tetrahydrofuran (100 mL) and methanol (100 mL) and to this solution was added p-toluenesulfonic acid (0.18 g, 0.95 mmol) and N-iodosuccinimide (17.8 g, 78.8 mmol). The solution was stirred all day. N-iodosuccinimide (0.78 g, 3.47 mmol) and p-toluenesulfonic acid (0.2 g, 1.05 mmol) were then added and the solution stirred overnight at room temperature under nitrogen. The solution was concentrated under vacuum to a small volume. Water (200 mL) was added to the reaction mixture and and a brown solid precipitated out. The solid was filtered- and washed with water, then dissolved in ethyl acetate (100 mL) and diethyl ether (60 mL). The organic solution was washed with 10% sodium thiosulfate solution (50 mL). This created an emulsion which was alleviated by adding diethy! ether and water and filtering undissolved material. The layers were separated and the organic layer was washed with 10% sodium thiosulfate solution (50 mL), water was then added to the aqueous layer and the layers separated. The organic layer was washed with brine (50 mL), dried over magnesium sulfate, filtered, and evaporated to yield the title compound as a brown solid that was dried under vacuum.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427682B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-31ef542d1c194f37aa38f494dbb023b1
출처 메모uspto-grants-2008_09