Reaction #985248

ord-e238337145c7482c9c9d51265af7417d

Reaction equation

c1ccncc1
pyridine
ClP(Cl)Cl
PCl3
[Al+3].[Cl-].[Cl-].[Cl-]
AlCl3
Fc1ccccc1
fluorobenzene
Fc1ccc(P(Cl)Cl)cc1
p-fluorophenyldichlorophosphine
Yield 47.0%

Reagents

None

Conditions

Temperature
60°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherA 1 l flask equipped with a thermostated jacket, mechanical stirring
  2. 2
    Temperaturethermometer and reflux condenser
  3. 3
    Othermist formed
  4. 4
    workup.STIRRINGStirring
  5. 5
    workup.WAITwas then continued at 60° C. for a further 30 min
  6. 6
    OtherAn irregular, large-lumped solid precipitated which could not
  7. 7
    Otherbe removed via a suction
  8. 8
    Filtrationfilter
  9. 9
    Filtrationonly by filtration
  10. 10
    FiltrationThe residue which was filtered off
  11. 11
    Washwas washed with petroleum ether
  12. 12
    WashThe filtrate and washing liquid
  13. 13
    workup.DISTILLATIONdistilled

Procedure

A 1 l flask equipped with a thermostated jacket, mechanical stirring, thermometer and reflux condenser was initially charged under an argon atmosphere with a mixture of 3.4 mol of PCl3 and 1.2 mol of AlCl3 (98% purity) at 73° C. 0.8 mol of fluorobenzene was then added within 30 min, while a weak argon stream was passed through the reaction flask. The reaction mixture was stirred for 3 hours and cooled to 60° C., and 1.25 mol of pyridine were added slowly within 45 min. The reaction was exothermic and mist formed. Stirring was then continued at 60° C. for a further 30 min. An irregular, large-lumped solid precipitated which could not be removed via a suction filter, but only by filtration. The residue which was filtered off was washed with petroleum ether. The filtrate and washing liquid were combined and distilled to obtain 73.3 g of p-fluorophenyldichlorophosphine in a yield of 47% of theory.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07351339B2uspto-grants-2008_04