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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 561797Erstellt: 25. Oktober 2026

Dimethylformamide → 5-bromo-2-chloro-N-cyclopropylbenzamide

https://huagongshe.com/reaction/561797

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt5-Bromo-2-chlorobenzoic acidHCID 33127—
EduktOxalyl chlorideHCID 65578—
EduktCyclopropylamineHCID 69828—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelTolueneHCID 1140—
Produkt5-bromo-2-chloro-N-cyclopropylbenzamideHCID 4806983—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a toluene solution (1 M) of 5-bromo-2-chlorobenzoic acid (1 eq.) and DMF (1.2 eq.) was added at 0° C. oxalyl chloride (1.2 eq.) dropwise over 1 h. The resulting solution was stirred at 0° C. for 2 h before the volatiles were removed in vacuo. The resulting residue was taken up in dichloromethane (1 M), cooled to 0° C. and added sequentially cyclopropylamine (1.5 eq.) and Hunig's base (2 eq.) dropwise over 1 h. The resulting suspension was stirred at RT for 18 h. The reaction was quenched with 1 N HCl and extracted with dichloromethane. The combined organic extracts were dried over MgSO4, filtered and the filtrate concentrated in vacuo to ˜⅓ in volume. The resulting white suspension was added an equivalent volume of hexanes and the title compound was isolated via vacuum filtration.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063105B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-ec6452fdf13347f698dfb0fc19b47127
Quellennotizuspto-grants-2011_11