Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70325Erstellt: 24. Oktober 2026

Nitrogen → 4'-Formyl-3-biphenylcarboxamide

https://huagongshe.com/de/reaction/70325

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktDichloromethaneHCID 6344—
EduktSodium CarbonateHCID 10340—
Edukt4-BromobenzaldehydeHCID 70741—
Edukt(3-Carbamoylphenyl)boronic acidHCID 2737814—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt4'-Formyl-3-biphenylcarboxamideHCID 59316529—

Reaktionsschritte

A mixture of 4-bromobenzaldehyde (2.78 g; 15.0 mmol), [3-(aminocarbonyl)-phenyl]boronic acid (2.72 g; 16.5 mmol), PdCl2(dppf).CH2Cl2 (0.306 g; 0.38 mmol), DME (25 mL) and Na2CO3 (25 mL of a 2M solution) was sparged 20 min with N2 and heated under reflux for 90 min (consumption of aryl bromide observed by LC/MS). Upon cooling, the mixture was partitioned between EtOAc/H2O, layers were separated, and the aqueous layer was extracted with EtOAc (×2). Combined organics were washed (H2O, brine), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography (EtOAc/hexanes), affording the title compound as a tan solid. LC/MS (method A) 1.91 min, m/z 226 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822518B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-f16869d2600a431382fa4e227ab303ab
Quellennotizuspto-grants-2014_09