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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1038662Erstellt: 26. Oktober 2026

4-Methyl-3-nitroaniline → N-(4-Methyl-3-nitrophenyl)-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1038662

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Methyl-3-nitroanilineHCID 8390—
EduktTriethylamineHCID 8471—
Edukt3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(4-Methyl-3-nitrophenyl)-3-(trifluoromethyl)benzamideHCID 11716802—

Reaktionsschritte

To a solution of 4-methyl-3-nitroaniline (5 g, 32.2 mmol, 1.0 eq.) and triethylamine (5.38 ml, 38.6 mmol, 1.2 eq.) in dichloromethane (100 ml) is added a solution of 3-trifluoromethylbenzoyl chloride 33.8 mmol, 1.05 eq.) within 30 min. The suspension formed is stirred for 1 h at room temperature. Then, the reaction mixture is diluted with dichloromethane (800 ml) and extracted with water (100 ml), 2M aqueous Na2CO3 (100 ml), 2M HCl (100 ml), water (100 ml). The organic layer is dried over Na2SO4, evaporated to a volume of about 100 ml and diluted with hexanes (100 ml). The precipitate is filtered off, washed with hexanes/dichloromethane 1:1 and hexanes. Vacuum drying over night at room temperatures gives light yellow fine needles: HPLC: tR=6.72 min (purity: >99%, gradient A), ESI-MS: 325.2 [MH]+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08552002B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-7f1ca51656ed403d8d5a940cc47138d5
Quellennotizuspto-grants-2013_10