Reaktion #42148

ord-142a14ae4f1c4556968ead328a5c1bc4

Lösungsmittel

Reaktionsbedingungen

Temperatur
25°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA 300-ml four-necked flask was equipped with a stirrer
  2. 2
    workup.STIRRINGthe mixture was stirred at 25° C. for 3 hours
  3. 3
    SonstigeAfter the completion of the reaction
  4. 4
    Filtrationthe precipitated product was filtered off
  5. 5
    SonstigeThe so obtained crystal
  6. 6
    Filtrationfiltered
  7. 7
    FiltrationThe product filtered off
  8. 8
    Waschenwas washed with 100 ml of toluene
  9. 9
    Sonstigewas then suspended in 100 ml of methanol at 50° C.
  10. 10
    Temperaturthe suspension was cooled to 25° C.
  11. 11
    Filtrationfiltered
  12. 12
    FiltrationThe product filtered off
  13. 13
    Waschenwas washed with 100 ml of methanol
  14. 14
    SonstigeThe crystal obtained
  15. 15
    Sonstigewas dried

Vorschrift

A 300-ml four-necked flask was equipped with a stirrer, a thermometer and a reflux condenser. 16.4 g (48 mmol) of sodium tetraphenylborate and 66 ml of water were weighed in the flask, followed by stirring to dissolve sodium tetraphenylborate. While the stirring was continuously carried out, the aqueous solution of tri-tert-butylphosphine sulfate was added to the solution, and the mixture was stirred at 25° C. for 3 hours. After the completion of the reaction, the precipitated product was filtered off. The so obtained crystal was suspended in 100 ml of toluene at 50° C., and the suspension was cooled to 25° C. and filtered. The product filtered off was washed with 100 ml of toluene. The crystal was then suspended in 100 ml of methanol at 50° C., and the suspension was cooled to 25° C. and filtered. The product filtered off was washed with 100 ml of methanol. The crystal obtained was dried to give 19.4 g of objective tri-tert-butylphosphonium tetraphenylborate as white crystal. The yield (mol %) was 93% based on tri-tert-butylphosphine.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728176B2uspto-grants-2010_06