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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439673Generated: October 26, 2026

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

https://huagongshe.com/reaction/439673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant4-Bromo-3-chloro-3,4,4-trifluorobutan-1-olHCID 21836477—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventDichloromethaneHCID 6344—
Product4-Bromo-3-chloro-3,4,4-trifluorobutanoic acidHCID 1091212785%

Reaction Steps

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 clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514717
Source datasetuspto-grants-1996_05
ORD IDord-77eaa78347e14d699c10a4101f11b5b8
Source noteuspto-grants-1996_05