Reaktion #1046

ord-b82f52deb4634a4bba0b118b41c64e02

Reaktionsgleichung

CC(C)(C)OP(=O)(CC(F)=C(F)F)OC(C)(C)C
di-t-butylphosphonate
CC(C)(C)OP(=O)(CC(F)=C(F)F)OC(C)(C)C
di-t-butyl 2,3,3-trifluoro-2-propenylphosphonate
Cl
HCl
O=P(O)(O)CC(F)=C(F)F
2,3,3-trifluoro-2-propenylphosphonic acid
Ausbeute 45.8%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe solution was concentrated
  2. 2
    workup.DISSOLUTIONthe residue was redissolved in 10 mL of water
  3. 3
    Waschenwashed with 10 mL of ether
  4. 4
    SonstigeEvaporation of the aqueous layer

Vorschrift

The above di-t-butylphosphonate (0.5 g) was dissolved in 3 mL of methanol and treated with 0.5 mL, of 3N HCl and allowed to stand at r.t. for 30 min. The solution was concentrated and the residue was redissolved in 10 mL of water and washed with 10 mL of ether. Evaporation of the aqueous layer gave 0.14 g of 2,3,3-trifluoro-2-propenylphosphonic acid as a yellow oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723470uspto-grants-1998_03