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HRID 13484作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfateHCID 6497—
反応物Trifluoroacetic anhydrideHCID 9845—
反応物Sodium HydroxideHCID 14798—
反応物TrifluoroacetamideHCID 67717—
反応物5-Fluoro-2-nitroanilineHCID 75399—
触媒Benzyltrimethylammonium chlorideHCID 5963—
溶媒TolueneHCID 1140—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物(5-Fluoro-2-nitrophenyl)methanamineHCID 22040333—

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728010B2
出典データセットuspto-grants-2010_06
ORD IDord-827e1e82bae44d098f4df3544470df9d
出典メモuspto-grants-2010_06