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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476322Generated: October 26, 2026

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

https://huagongshe.com/reaction/476322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Bis(dichlorophosphino)benzeneHCID 3316562—
ReactantHCID 178418676HCID 178418676—
SolventTetrahydrofuranHCID 8028—
Product1,2-Bis(bis(4-fluorophenyl)phosphino)benzeneHCID 5293791262%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637710B2
Source datasetuspto-grants-2014_01
ORD IDord-e2887f65a4a64def8574959fa4dd001b
Source noteuspto-grants-2014_01