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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13484Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktTrifluoroacetic anhydrideHCID 9845—
EduktSodium HydroxideHCID 14798—
EduktTrifluoroacetamideHCID 67717—
Edukt5-Fluoro-2-nitroanilineHCID 75399—
KatalysatorBenzyltrimethylammonium chlorideHCID 5963—
LösungsmittelTolueneHCID 1140—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
Produkt(5-Fluoro-2-nitrophenyl)methanamineHCID 22040333—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728010B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-827e1e82bae44d098f4df3544470df9d
Quellennotizuspto-grants-2010_06