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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 439673Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/439673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
Edukt4-Bromo-3-chloro-3,4,4-trifluorobutan-1-olHCID 21836477—
EduktJones' reagentHCID 131709961—
LösungsmittelAcetoneHCID 180—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Bromo-3-chloro-3,4,4-trifluorobutanoic acidHCID 1091212785%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05514717
Quelldatensatzuspto-grants-1996_05
ORD IDord-77eaa78347e14d699c10a4101f11b5b8
Quellennotizuspto-grants-1996_05