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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256617Generated: November 4, 2026

Methyl iodide → N-Methyl-2-nitro-4-(trifluoromethoxy)aniline

https://huagongshe.com/reaction/1256617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Nitro-4-(trifluoromethoxy)anilineHCID 2775772—
SolventDimethylformamideHCID 6228—
ProductN-Methyl-2-nitro-4-(trifluoromethoxy)anilineHCID 5321687576.3%

Reaction Steps

To a mixture of 2.22 g of 2-nitro-4-trifluoromethoxyaniline and 20 ml of DMF was added 0.44 g of sodium hydride (60% oily), and the mixture was stirred for 10 minutes under ice cool. To this mixture was added 1.42 g of methyl iodide, then, the mixture was stirred for 1 hour at room temperature. Into the reaction mixture, a saturated ammonium chloride aqueous solution was poured, and the mixture was extracted three times with ethyl acetate. The organic layer was dried over magnesium sulfate, then, concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.80 g of N-methyl-2-nitro-4-trifluoromethoxyaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461181B2
Source datasetuspto-grants-2013_06
ORD IDord-2c8ad0f26c45424e934a1ca4998020e2
Source noteuspto-grants-2013_06