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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9559Erstellt: 25. Oktober 2026

Pyridiniumtribromide → 2-Bromo-1-(3-methyl-4'-nitro-1,1'-biphenyl-4-yl)ethanone

https://huagongshe.com/reaction/9559

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridiniumtribromideHCID 21124087—
Edukt1-(3-Methyl-4'-nitro-1,1'-biphenyl-4-yl)ethanoneHCID 21985798—
LösungsmittelAcetic AcidHCID 176—
Produkt2-Bromo-1-(3-methyl-4'-nitro-1,1'-biphenyl-4-yl)ethanoneHCID 2198568859%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

A mixture of 1-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)ethanone (5.66 g, 22 mmol), pyridinium tribromide (10.63 g, 33.0 mmol), and glacial acetic acid (60 mL) was stirred at 110° C. for 3 h. The reaction mixture was cooled to 0–5° C., and the precipitated product was collected by filtration and washed with small amounts of water, ethanol, and diethyl ether. The crude material was purified by flash chromatography (5:95 ethyl acetate/hexane) to give 2-bromo-1-(3-methyl-4′-nitro-1,1′-biphenyl-4-yl)ethanone as a light yellow solid (4.33 g, 59% yield). HPLC ret. time 3.63 min; 1H NMR (CDCl3) δ: 2.63 (s, 3H), 2.25 (s, 2H), 7.52–7.58 (m, 2H), 7.72–7.83 (m, 3H), 8.32 (d, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091228B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-1babce0031024287921edca41706873d
Quellennotizuspto-grants-2006_08