Reacción #985248
ord-e238337145c7482c9c9d51265af7417d
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1OtroA 1 l flask equipped with a thermostated jacket, mechanical stirring
- 2Temperaturathermometer and reflux condenser
- 3Otromist formed
- 4workup.STIRRINGStirring
- 5workup.WAITwas then continued at 60° C. for a further 30 min
- 6OtroAn irregular, large-lumped solid precipitated which could not
- 7Otrobe removed via a suction
- 8Filtraciónfilter
- 9Filtraciónonly by filtration
- 10FiltraciónThe residue which was filtered off
- 11Lavadowas washed with petroleum ether
- 12LavadoThe filtrate and washing liquid
- 13workup.DISTILLATIONdistilled
Procedimiento
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.