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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77723Erstellt: 26. Oktober 2026

3-(Trifluoromethyl)aniline → 3-iodo-4-methyl-N-(3-(trifluoromethyl)phenyl)benzamide

https://huagongshe.com/reaction/77723

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Trifluoromethyl)anilineHCID 7375—
EduktOxalyl chlorideHCID 65578—
EduktDiisopropylethylamineHCID 81531—
Edukt3-Iodo-4-methylbenzoic acidHCID 621640—
KatalysatorDimethylformamideHCID 6228—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-iodo-4-methyl-N-(3-(trifluoromethyl)phenyl)benzamideHCID 17197569—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a suspension of 3-iodo-4-methylbenzoic acid (3.00 g, 11.4 mmol) in DCM (30 mL) at 0° C. was added oxalyl chloride (1.45 mL, 17.2 mmol) followed by two drops of DMF. The reaction was stirred at 0° C. for 30 minutes followed by warming to ambient temperature for 40 minutes. The mixture was concentrated in vacuo. To the resulting residue was added DCM (30 mL), DIPEA (2.99 mL, 17.2 mmol) and 3-(trifluoromethyl)-benzenamine (1.42 mL, 11.4 mmol). The reaction was stirred at ambient temperature for 1 hour. The mixture was then poured into water, and the product was extracted with DCM. The combined organic extracts were washed with water, followed by saturated sodium bicarbonate, and then dried over sodium sulfate. An equal volume of hexane was added and most of the DCM was then removed in vacuo. The resulting yellow solid was filtered, rinsed with hexane and air dried. (4.27 g, 92%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841318B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-4dcd7be8c7164f178f5cc798c710ebad
Quellennotizuspto-grants-2014_09