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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971468Generated: October 26, 2026

Methanol → N-(dimethylamino)-2,6-dinitro-3-methoxy-4-trifluoromethylaniline

https://huagongshe.com/reaction/971468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium ChlorideHCID 5234—
ReactantSodium MethoxideHCID 10942334—
ReactantN-dimethylamino-3-chloro-2,6-dinitro-4-trifluoromethylanilineHCID 13101276—
SolventWaterHCID 962—
ProductN-(dimethylamino)-2,6-dinitro-3-methoxy-4-trifluoromethylanilineHCID 13101285—

Reaction Steps

To a stirred solution of 5.0 g. (0.015 mole) of N-(dimethylamino)-3-chloro-2,6-dinitro-4-trifluoromethylaniline and 50 ml. of anhydrous methanol was added 3.77 g. (0.015 mole) of a 21.8% methanolic sodium methoxide solution. The resultant mixture was stirred at room temperature for 6 hours and was then refluxed overnight for 16 hours. The methanol was then evaporated under vacuum leaving a yellow-solid residue. To the residue was added 150 ml. of water and the mixture stirred for 30 minutes to dissolve the NaCl and any other water-soluble materials. The mixture was then filtered and the water-insoluble solids were washed well with water. The solids were then dissolved in 30 ml. of refluxing 95% ethanol. On cooling, the product crystallized and was isolated by filtration to give 3.83 g. (77.7%) of a yellow crystalline solid; m.p. 109°-110.5° C. After recrystallization from 95% ethanol, the product melts at 110°-111.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160090
Source datasetuspto-grants-1979_07
ORD IDord-813bdfdc260e45aa9a7f0baa50870c68
Source noteuspto-grants-1979_07