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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461259Generated: November 2, 2026

Methyl iodide → N-ethoxalyl-N-methyl-4-chloro-6-nitro-2-trifluoromethylaniline

https://huagongshe.com/reaction/1461259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5-Chloro-2-ethoxalylamino-3-nitrobenzotrifluorideHCID 19980305—
SolventDimethylformamideHCID 6228—
ProductN-ethoxalyl-N-methyl-4-chloro-6-nitro-2-trifluoromethylanilineHCID 19980279—

Reaction Steps

To a stirred solution of N-ethoxalyl-4-chloro-6-nitro-2-trifluoromethylaniline (11 g. 32.3 mmol) and methyl iodide (3.0 ml, 48 mmol) in dry dimethylformamide (DMF, 50 ml) was added in portions sodium hydride (total 1.7 g, 39 mmol). External cooling was used to keep the reaction temperature below 25° C. Stirring was continued at room temperature for 3 h, whereafter the solvent was removed by evaporation in vacuo. The residue was then partitioned between ether and water. The organic phase was washed twice with water, dried over Na2SO4 and evaporated. This treatment left the title compound as an oil, which was processed without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05075304
Source datasetuspto-grants-1991_12
ORD IDord-7a75cf8b2a6a482fadcb91870baa8a3e
Source noteuspto-grants-1991_12