Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257250Erstellt: 24. Oktober 2026

1-Bromo-2-nitrobenzene → 4'-Methyl-2-nitro-1,1'-biphenyl

https://huagongshe.com/de/reaction/257250

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-2-nitrobenzeneHCID 11341—
EduktPotassium HydroxideHCID 14797—
EduktStannane, trimethyl(4-methylphenyl)-HCID 617834—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt4'-Methyl-2-nitro-1,1'-biphenylHCID 1044319490%

Reaktionsschritte

A solution of 5.0 g (19.6 mmol) 4-(trimethylstannyl)toluene, 4.08 g (20.2 mmol) 1-bromo-2-nitrobenzene, and 138 mg (0.2 mmol) bis(triphenylphosphine)palladium(II) chloride in 100 mL DMF was heated to 110° C. for 4 hours. The mixture was cooled to room temperature, was poured into a mixture of brine and 1N KOH, then was extracted 3 times with ether. The combined organic material was washed with 1N KOH, was washed with brine, was dried over magnesium sulfate, was stripped of solvent in vacuo, and was chromatographed on silica gel under medium pressure using 5% ethyl acetate in hexanes to give 3.76 g (90% yield) of the title compound as a light lemon-yellow colored oil. Rf 0.31 in 10% EtOAc/hexane, visualized by UV and ammonium molybdate/ceric sulfate stain.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05260285
Quelldatensatzuspto-grants-1993_11
ORD IDord-17845e8d170b4f5da9badba8d0bdeeb6
Quellennotizuspto-grants-1993_11