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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 389089Erstellt: 25. Oktober 2026

Triethylamine → 4-fluoro-N-methyl-2-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/389089

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt4-Fluoro-2-(trifluoromethyl)benzoic acidHCID 688255—
EduktMethylamine tetrahydrofuranHCID 66615946—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-fluoro-N-methyl-2-(trifluoromethyl)benzamideHCID 22095075—

Reaktionsschritte

DMF (3 drops) and oxalyl chloride (2.55 ml) were added to a mixture of 4-fluoro-2-(trifluoromethyl)benzoic acid (5.50 g) and dichloromethane (50 ml), followed by stirring at room temperature for 3 hours. The reaction solution was added dropwise to a 2M methylamine-THF solution (17.3 ml) and a solution of triethylamine (5.55 ml) in dichloromethane (50 ml) under ice cooling, followed by stirring for 30 minutes and concentration under reduced pressure, addition of water and extraction with ethyl acetate. The organic layer was washed with water, saturated aqueous sodium bicarbonate solution and then saturated brine in this order, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was washed with diisopropylether to obtain 4-fluoro-N-methyl-2-(trifluoromethyl)benzamide (4.37 g) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08377923B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-d0fb158523c248fca59354d4fe3383c2
Quellennotizuspto-grants-2013_02