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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 405692Erstellt: 25. Oktober 2026

Triphenylphosphine → 1-(4-Bromo-3-methyl-phenyl)-2-(triphenylphosphanylidene)-ethanone

https://huagongshe.com/reaction/405692

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktSodium BicarbonateHCID 516892—
Edukt2-Bromo-1-(4-bromo-3-methylphenyl)ethanoneHCID 59166346—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-(4-Bromo-3-methyl-phenyl)-2-(triphenylphosphanylidene)-ethanoneHCID 86674671—

Reaktionsschritte

1300 mg of 2-Bromo-1-(4-bromo-3-methyl-phenyl)-ethanone (VIIa) (Journal of Organic Chemistry (1947), 12, 617-703) was stirred with 1300 mg of triphenylphosphine in 20 ml of dichloromethane at ambient temperature for 18 hours. The mixture was diluted with toluene and the separated phosphonium salt was filtered off. It was then suspended in 20 ml of dichloromethane and 20 ml of water. 800 mg (7.55 mmol) of sodium bicarbonate was then added in 20 ml of water and the mixture was stirred overnight. The organic layer was separated, dried and evaporated under reduced pressure. The residue was triturated with hexane giving 1.6 g (86%) of 1-(4-Bromo-3-methyl-phenyl)-2-(triphenylphosphanylidene)-ethanone (Va) as a solid. 1H-NMR (CDCl3, δ in ppm): 7.40-7.90 (m, 18H), 4.40 (m, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754053B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-378b5957ca814ec68c328221864c4604
Quellennotizuspto-grants-2014_06