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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13484생성일: 2026년 10월 23일

Dimethyl Sulfate → (5-Fluoro-2-nitrophenyl)methanamine

https://huagongshe.com/ko/reaction/13484

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfateHCID 6497—
반응물Trifluoroacetic anhydrideHCID 9845—
반응물Sodium HydroxideHCID 14798—
반응물TrifluoroacetamideHCID 67717—
반응물5-Fluoro-2-nitroanilineHCID 75399—
촉매Benzyltrimethylammonium chlorideHCID 5963—
용매TolueneHCID 1140—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물(5-Fluoro-2-nitrophenyl)methanamineHCID 22040333—

반응 조건

온도0 °C

반응 단계

A solution of 5-fluoro-2-nitrophenylamine (1 eq) in methylenechloride was treated with trifluoroacetic anhydride (1 eq) and stirred for 10 minutes at 0° C. The mixture was quenched with saturated sodium bicarbonate solution. The organic layer was separated and washed with water, brine, dried and evaporated. To the solution of the trifluoroacetamide (1 eq) in a mixture of toluene, acetonitrile and sodium hydroxide solution (50%) was added benzyltrimethylammonium chloride (1 eq) and dimethyl sulfate (1.2 eq). The biphasic mixture was stirred overnight at room temperature and evaporated. The mixture was taken up in ethyl acetate, washed with water, brine, dried and evaporated. The crude was purified by column chromatography eluting with 1:1 hexanes and ethyl acetate to afford (5-fluoro-2-nitrophenyl)methylamine. MS: MH+=170.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728010B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-827e1e82bae44d098f4df3544470df9d
출처 메모uspto-grants-2010_06