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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 859795Erstellt: 25. Oktober 2026

Cesium carbonate → Methyl 5'-amino-2'-methyl-1,1'-biphenyl-4-carboxylate

https://huagongshe.com/reaction/859795

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt4-Methoxycarbonylphenylboronic acidHCID 2734369—
EduktMethyl 5'-amino-2'-methyl-1,1'-biphenyl-4-carboxylate 3-Bromo4-methylanilineHCID 69203176—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
ProduktMethyl 5'-amino-2'-methyl-1,1'-biphenyl-4-carboxylateHCID 2109058351,8%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Methyl 5′-amino-2′-methyl-1,1′-biphenyl-4-carboxylate 3-Bromo-4-methylaniline (744 mg, 4.0 mmol), (4-methoxycarbonylphenyl)boronic acid (864 mg, 4.8 mmol), tetrakis(triphenylphosphine)palladium (100 mg, 0.087 mmol) and caesium carbonate (2.4 g, 7.37 mmol) were mixed in DME (30 ml) and heated at 90° C. for 20 h. The reaction was absorbed onto silica applied to a silica SPE (10 g) and eluted with ethyl acetate/cyclohexane (0–100% ethyl acetate). The solvent was evaporated from the product fractions under vacuum to give methyl 5′-amino-2′-methyl-1,1′-biphenyl-4-carboxylate (500 mg, 43%). NMR; δH CDCl3 8.07,(2H, d), 7.38,(2H, d), 7.07,(1H, d), 6.67,(1H, dd), 6.60,(1H, d), 3.94,(3H, s), 2.14,(3H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07151118B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-4eba057983bf49d59a3d8c9d08c38479
Quellennotizuspto-grants-2006_12