Isopropanol → 4-Bromo-3-chloro-3,4,4-trifluorobutanoic acid

HRID 2394970Notes

Reaction equation

HRID 2394970 reaction equation
[Br:1][C:2]([F:10])([F:9])[C:3]([Cl:8])([F:7])[CH2:4][CH2:5][OH:6].CC(C)=[O:13].OS(O)(=O)=O.O=[Cr](=O)=O.C(O)(C)C>CC(C)=O.C(Cl)Cl>[Br:1][C:2]([F:10])([F:9])[C:3]([Cl:8])([F:7])[CH2:4][C:5]([OH:13])=[O:6]

Participants

6

Procedure

A solution of 4-bromo-3-chloro-3,4,4-trifluorobutanol (IX) (2.41 g, 10 mmol) in acetone (35 mL) was treated with Jones reagent (7.5 mL) in 10 min with stirring and cooling (ice-water bath). The mixture was then stirred at room temperature for 30 min and 0.5 mL of i-propanol was then added. The precipitated salts were removed by filtration, washed with acetone. The residue obtained after concentration of the filtrate was dissolved in methylene chloride (100 mL), washed with 1N HCl (50 mL), brine, and dried over anhydrous magnesium sulfate. Evaporation of the solvent gave 2.17 g (85%) of 4-bromo-3-chloro-3,4,4-trifluorobutanoic acid (VIII) as a dear oil.

Workup

  1. stirringThe mixture was then stirred at room temperature for 30 min
  2. customThe precipitated salts were removed by filtration
  3. washwashed with acetone
  4. customThe residue obtained after concentration of the filtrate
  5. washwashed with 1N HCl (50 mL), brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customEvaporation of the solvent

Sources & evidence

ORD record
ord-29cf10cc80ee4fee8a2c21e97af1b7e4
Source dataset
uspto-grants-1998_09
Patent number
US05811578

Reaction notes

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