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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 619974Erstellt: 25. Oktober 2026

alpha,alpha,alpha,3-Tetrafluorotoluene → 2-Fluoro-6-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/619974

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktalpha,alpha,alpha,3-TetrafluorotolueneHCID 67867—
EduktDry ice diethyl etherHCID 86742199—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Fluoro-6-(trifluoromethyl)benzoic acidHCID 688123—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A mixture of 3-fluorobenzotrifluoride (25.0 g, 0.15 mol) in tetrahydrofuran (200 ml) was cooled to -78° C. in a dry ice/acetone bath under nitrogen atmosphere. To this solution was added dropwise with rapid stirring N-butyl lithium (1.6M, 95.2 ml) at such rate that the temperature did not exceed -60° C. When the addition was complete, the mixture was allowed to stir at -78° C. for an additional five hours. The mixture was then poured over a slurry of dry ice/ether and allowed to come to room temperature. The solvent was removed by evaporation under reduced pressure to obtain a white solid residue. This solid was dissolved in a minimum amount of water, the solution was extracted with diethyl ether (2×100 ml) and the aqueous phase was acidified to pH 2 with dilute hydrochloric acid. An oil formed and this was dissolved in diethyl ether; the solution was washed several times with water and dried over magnesium sulfate. The solvent was removed by evaporation under reduced pressure to give a white solid. NMR analysis indicated this product was a mixture of the title compound and an isomer. A yield of 15.6 g (50 percent of theory) was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04818273
Quelldatensatzuspto-grants-1989_04
ORD IDord-8dd6a32c9b7b462e99f7be7371ab3f7b
Quellennotizuspto-grants-1989_04