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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 371690Erstellt: 25. Oktober 2026

Ethanol → Benzenamine, N-methoxy-2,6-dinitro-4-(trifluoromethyl)-

https://huagongshe.com/reaction/371690

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktTriethylamineHCID 8471—
Edukt4-Chloro-3,5-dinitrobenzotrifluorideHCID 9809—
EduktO-Methylhydroxylamine hydrochlorideHCID 521874—
LösungsmittelEthyl AcetateHCID 8857—
ProduktBenzenamine, N-methoxy-2,6-dinitro-4-(trifluoromethyl)-HCID 12102672—

Reaktionsschritte

To a solution prepared from 27.0 g. (0.1 mole) of 4-chloro-3,5-dinitrobenzotrifluoride in 200 ml. of ethanol there was added 25.25 g. (0.25 mole) of triethylamine, and 12.5 g. (0.15 mole) of methoxyamine hydrochloride. Upon the addition of the methoxyamine hydrochloride, the temperature of the reaction mixture rose to about 50° C. The reaction mixture was allowed to stir for about 11/2 hours and the reaction product mixture was worked up by diluting with ethyl acetate, washing several times with dilute hydrochloric acid and water, and drying the organic layer over anhydrous magnesium sulfate. The drying agent was filtered off and the filtrate concentrated on the steam bath to leave a residue. The residue was allowed to chill over the weekend in the refrigerator and crystals separated. The crystalline product was filtered off. It had a melting point of about 135°-137° C., weighed 21.0 g., and was identified by NMR spectrum and elemental analyses as 2,6-dinitro-N-methoxy-α,α,α-trifluoro-p-toluidine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04087460
Quelldatensatzuspto-grants-1978_05
ORD IDord-751c3818556047f8824abb978828dfb8
Quellennotizuspto-grants-1978_05