Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270698Erstellt: 26. Oktober 2026

2-Aminobenzaldehyde → 2-(2,6-dichloro-3-nitro-phenyl)-N-(2-formyl-phenyl)-acetamide

https://huagongshe.com/reaction/270698

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminobenzaldehydeHCID 68255—
Edukt2,6-Dichloro-3-nitrophenylacetic acidHCID 54265437—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelThionyl ChlorideHCID 24386—
Produkt2-(2,6-dichloro-3-nitro-phenyl)-N-(2-formyl-phenyl)-acetamideHCID 5983388288,6%

Reaktionsschritte

A solution of (2,6-dichloro-3-nitro-phenyl)-acetic acid (0.90 g, 3.35 mmol) in thionyl chloride (15 mL) is refluxed for one hour. The solvent is removed by concentration and dry toluene is added to thoroughly remove thionyl chloride. To the solution of acid chloride in dry dichloromethane (30 mL) is added (drop-wise) a solution of 2-aminobenzaldehyde (0.365 g, 3.02 mmol) in dichloromethane (5.0 mL). The mixture is stirred at room temperature for 2 hours. The reaction mixture is diluted with EtOAc and washed with saturated K2CO3 and brine. The organic layer is dried, filtered and concentrated to give crude product (0.94 g, 88.6%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07449582B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-85921cc9266e4e75939cb8df0dbc30ea
Quellennotizuspto-grants-2008_11