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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 436350Erstellt: 25. Oktober 2026

Benzene → 1,2-Bis(o-anisylphenylphosphino) ethane

https://huagongshe.com/reaction/436350

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktTriethylamineHCID 8471—
EduktTrichlorosilaneHCID 24811—
Edukt1,2-Bis(o-anisylphenylphosphinyl) ethaneHCID 86734501—
LösungsmittelMethanolHCID 887—
LösungsmittelAcetonitrileHCID 6342—
Produkt1,2-Bis(o-anisylphenylphosphino) ethaneHCID 15061558—

Reaktionsschritte

Reduction of 1,2-bis(o-anisylphenylphosphinyl) ethane was accomplished by refluxing 16.5 g. (.12 mole) trichlorosilane and 12.2 g. (.12 mole) triethylamine in 188 ml. of dry benzene for one hour. Then 3.0 g. (.012 mole) of 1,2-bis(o-anisylphenylphosphinyl) ethane in 75 ml. of dry acetonitrile was added and the mixture refluxed 1.5 hours. Quenching in 30% sodium hydroxide solution followed by separating and evaporating the organic layer gave 1.4 g. of crude crystals which were insoluble in cold methanol. Further crystallization from hot methanol gave 1,2-bis(o-anisylphenylphosphino) ethane, m.p. 102°-104° C., [α]D20 - 83.4° (C = 0.5 in CHCl3). The mass spectra gave a very strong parent peak at 458 and the nmr confirmed the structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04008281
Quelldatensatzuspto-grants-1977_02
ORD IDord-907d81b6612b48c0bc4d1749cb8cd83e
Quellennotizuspto-grants-1977_02