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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1613963Erstellt: 26. Oktober 2026

1-Chloro-2-(trifluoromethyl)benzene → 2-(Trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1613963

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Chloro-2-(trifluoromethyl)benzeneHCID 6921—
EduktPotassium CarbonateHCID 11430—
EduktHCID 178418416HCID 178418416—
KatalysatorPalladium ChlorideHCID 24290—
KatalysatorChiraphosHCID 3882352—
LösungsmittelWaterHCID 962—
Produkt2-(Trifluoromethyl)benzoic acidHCID 989991,5%

Reaktionsbedingungen

Temperatur240 °C

Reaktionsschritte

In an autoclave made of metal were placed 18 g of ortho-chlorobenzotrifluoride, 3.5 mg of palladium chloride, 170 mg of bisdiphenylphosphinobutane and 3.1 g of potassium carbonate. The air in the autoclave was replaced with carbon monoxide introduced thereinto in several times, after which carbon monoxide was further introduced to adjust its pressure therein to 30 kg/cm2. The reaction was carried out with stirring on a salt bath at a bath temperature of 240° C. After completion of the reaction, the reaction mixture was cooled to room temperature and water was added. The aqueous layer was separated and then acid was added thereto, followed by extraction from the aqueous layer. The ether layer was dried and then concentrated to obtain 3.9 g of ortho-trifluoromethylbenzoic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05194631
Quelldatensatzuspto-grants-1993_03
ORD IDord-a96233ecf6c3490fac4a02b62c4ef30e
Quellennotizuspto-grants-1993_03