Hydrochloric Acid → 2,3,3-Trifluoro-2-propenylphosphonic acid

HRID 1779358Notes

Reaction equation

HRID 1779358 reaction equation
[F:1][C:2](=[C:16]([F:18])[F:17])[CH2:3][P:4](=[O:15])([O:10]C(C)(C)C)[O:5]C(C)(C)C.Cl>CO>[F:1][C:2](=[C:16]([F:18])[F:17])[CH2:3][P:4](=[O:5])([OH:15])[OH:10]

Participants

4

Procedure

The above di-t-butylphosphonate (0.5 g) was dissolved in 3 mL of methanol and treated with 0.5 mL of 3 N 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.

Workup

  1. concentrationThe solution was concentrated
  2. dissolutionthe residue was redissolved in 10 mL of water
  3. washwashed with 10 mL of ether
  4. customEvaporation of the aqueous layer

Sources & evidence

ORD record
ord-cc5925a40fb34c5c8ca3f970452f82bf
Source dataset
uspto-grants-1997_05
Patent number
US05627174

Reaction notes

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