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HRID 1673253Erstellt: 24. Oktober 2026

Ethanone, 1-(2-chlorophenyl)- → 2-[4-Chloro-3-(methyloxy)phenyl]-1-(2-chlorophenyl)-ethanone

https://huagongshe.com/de/reaction/1673253

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanone, 1-(2-chlorophenyl)-HCID 72864—
Edukt2-(Dicyclohexylphosphino)-2'-methylbiphenylHCID 2734938—
Edukt5-Bromo-2-chloroanisoleHCID 2769567—
EduktSodium t-butoxideHCID 23676156—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelTolueneHCID 1140—
Produkt2-[4-Chloro-3-(methyloxy)phenyl]-1-(2-chlorophenyl)-ethanoneHCID 67330467—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 1-(2-chlorophenyl)ethanone (1.4 mL, 10.8 mmol), 4-bromo-1-chloro-2-(methyloxy)benzene (2.0 g, 9.0 mmol), sodium tert-butoxide (2.2 g, 22.6 mmol), palladium(II) acetate (20.3 mg, 0.1 mmol), and 2-(dicyclohexylphosphino)-2′-methylbiphenyl (65.8 mg, 0.2 mmol) in 30 mL of toluene was degassed and stirred at 80° C. for 16 h. The reaction mixture was cooled and a mixture of Et2O (100 mL) and H2O (100 mL) was added. The aq layer was separated and extracted with Et2O (3×50 mL). Organic layers were combined, dried over MgSO4, and concentrated. Chromatography on a Biotage 40+M cartridge using 1:9 v/v EtOAc/hexanes as the eluant afforded the product: 1H NMR δ 3.87 (s, 3H), 4.22 (s, 2H), 6.75 (dd, J=1.7, 8.2, 1H), 6.81 (d, J=1.6, 1H), 7.26-7.31 (m, 2H), 7.37-7.43 (m, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07999107B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-232b8803963f40f0a7456c432aca91f1
Quellennotizuspto-grants-2011_08