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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 219774Erstellt: 24. Oktober 2026

Sodium Hydroxide → 3-Methyl-4-[2-(trifluoromethyl)phenyl]benzoic acid

https://huagongshe.com/de/reaction/219774

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktMethyl 2-methyl-2'-(trifluoromethyl)biphenyl-4-carboxylateHCID 59606539—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt3-Methyl-4-[2-(trifluoromethyl)phenyl]benzoic acidHCID 2194781284%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of methyl 2-methyl-2′-(trifluoromethyl)biphenyl-4-carboxylate, prepared in step 1 (3 g; 10.19 mmol; 1 eq.) in EtOH (90 mL), was added at RT an aqueous solution of sodium hydroxide (6.12 mL; 5 M; 30.58 mmol; 3 eq.). The reaction mixture was stirred at 60° C. for one hour. The reaction mixture was concentrated under vacuum to give a brown solid. It was taken up in water (400 mL) and the aqueous phase was washed twice with EtOAc (200 mL). Aqueous phase was acidified with concentrated HCl (2 mL) to pH 2. Then it was concentrated under vacuum until a precipitate was formed (⅓ of volume). The suspension was filtered off and dried under vacuum, affording the title compound as a beige solid (2.41 g, 84%). 1H NMR: (DMSO-d6, 300 MHz) δ 13.03 (s, 1H), 7.91-7.68 (m, 5H), 7.38-7.36 (d, J=8.27 Hz, 1H), 7.27-7.25 (d, J=8.24 Hz, 1H), 2.05 (s, 3H). LC/MS (Method A): 279.0 (M−H)−. HPLC (Method A) Rt 4.49 min (Purity: 95.7%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202865B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-50b1b3cf03a945c0a25f99461b0a7743
Quellennotizuspto-grants-2012_06