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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13484Generated: October 26, 2026

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

https://huagongshe.com/reaction/13484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium HydroxideHCID 14798—
ReactantTrifluoroacetamideHCID 67717—
Reactant5-Fluoro-2-nitroanilineHCID 75399—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product(5-Fluoro-2-nitrophenyl)methanamineHCID 22040333—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728010B2
Source datasetuspto-grants-2010_06
ORD IDord-827e1e82bae44d098f4df3544470df9d
Source noteuspto-grants-2010_06