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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 476322Erstellt: 24. Oktober 2026

1,2-Bis(dichlorophosphino)benzene → 1,2-Bis(bis(4-fluorophenyl)phosphino)benzene

https://huagongshe.com/de/reaction/476322

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-Bis(dichlorophosphino)benzeneHCID 3316562—
EduktHCID 178418676HCID 178418676—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1,2-Bis(bis(4-fluorophenyl)phosphino)benzeneHCID 5293791262%

Reaktionsschritte

A THF solution (26.6 mL, 1.03 M, 27.40 mmol) of p-fluorophenylmagnesium bromide was added to a mixture of 1,2-bis(dichlorophosphino)benzene (0.96 g, 3.43 mmol) and THF (20 mL) in an argon atmosphere at −78° C. After warming to room temperature, the mixture was allowed to react overnight at 60° C. The reaction mixture was cooled to ambient temperature, and the solvent was removed under reduced pressure; subsequently, CH2Cl2 (30 mL) was added. 1N aqueous solution of hydrochloric acid (20 mL) was added to the reaction mixture, and the aqueous layer was extracted three times with CH2Cl2. The moisture contained in the combined organic extract was removed with magnesium sulfate, and the extract was filtered. After removing the solvent under reduced pressure, the resulting yellow oily substance was triturated with methanol to give a white powder, and the white powder was washed two times with methanol, giving the title compound as a white powder (1.10 g, yield 62%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08637710B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-e2887f65a4a64def8574959fa4dd001b
Quellennotizuspto-grants-2014_01