Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1796502Erstellt: 26. Oktober 2026

Diethylamine → N,N-Diethyl-3-fluoro-4-nitrobenzamide

https://huagongshe.com/reaction/1796502

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethylamineHCID 8021—
EduktTriethylamineHCID 8471—
Edukt3-Fluoro-4-nitrobenzoic acidHCID 230653—
EduktDCM thionyl chlorideHCID 21879677—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN,N-Diethyl-3-fluoro-4-nitrobenzamideHCID 2218141779%

Reaktionsschritte

3-Fluoro-4-nitrobenzoic acid (5.0 g, 27.0 mmol) was refluxed in a mixture of 2:1 CH2Cl2/SOCl2 (150 mL) overnight. The solvent was concentrated and the residue dissolved in CH2Cl2 (50 mL). Another CH2Cl2 solution (50 mL) of diethylamine (3.35 mL, 1.2 eq) and triethylamine (7.5 mL, 2 eq) was then added dropwise to the cold stirring solution (0° C.) of the acid chloride. The solution was stirred at rt for 1 h. The solution was then washed with 5% KHSO4 solution, saturated NaHCO3 solution, brine and dried over anhydrous MgSO4. The crude product was purified by flash chromatography using 2:1/hex:EtOAc on silica gel to afford the title compound (5.10 g, 79% yield); 1H NMR (400 MHz, CDCl3) δ 8.12 (m, 1H), 7.29 (m, 2H), 3.56 (br d, 2H), 3.23 (br d, 2H), 1.27 (br s, 3H), 1.15 (br s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07030139B2
Quelldatensatzuspto-grants-2006_04
ORD IDord-feaba13bf5764cc58651cc296afbd091
Quellennotizuspto-grants-2006_04