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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630995Generated: October 31, 2026

Potassium Carbonate → 3-Methyl-4-[2-(trifluoromethyl)phenyl]benzoic acid

https://huagongshe.com/reaction/1630995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant2-(Trifluoromethyl)benzeneboronic acidHCID 2734387—
ReactantMethyl 4-bromo-3-methylbenzoateHCID 3294148—
CatalystBis(tricyclohexylphosphine)palladium(II) DichlorideHCID 11556747—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-Methyl-4-[2-(trifluoromethyl)phenyl]benzoic acidHCID 2194781292%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of methyl 4-bromo-3-methylbenzoate (20.0 g, 87.3 mmol), 2-(trifluoromethyl)benzeneboronic acid (24.9 g, 131.0 mmol), potassium carbonate (24.1 g, 174.6 mmol) and bis(tricyclohexylphosphine)palladium (II) dichloride (64.5 mg, 0.09 mmol) was prepared in dioxane (200 mL) and water (50 mL) under N2 atmosphere. The mixture was heated at 100° C. for 3 hours. A 5N aqueous solution of NaOH (100 mL) was added and the reaction mixture was stirred at 100° C. for one additional hour. The reaction mixture was cooled at RT and the aqueous layer was removed. The organic layer was filtered through a Celite pad, concentrated until 75 ml under reduced pressure, diluted with water (125 ml) and washed with MTBE (2×200 mL). The aqueous layer was acidified with a 5N aqueous solution of HCl (25 ml, pH˜1) and extracted with MTBE (2×100 ml). The organic layers were combined, dried (Na2SO4) and filtered through a Celite pad. The solution was concentrated until 100 mL, then heptane was added (200 mL). The mixture was concentrated until 100 mL. The precipitate was filtered off and rinsed twice with heptane, then dried under reduced pressure to give the title compound as a white powder (22.5 g, 92%). HPLC (Method A), Rt: 4.4 min (purity: 100%). UPLC/MS, M−(ESI): 279.0. 1H NMR (DMSO-d6, 300 MHz) δ 13.00 (s, 1H), 7.87 (m, 2H), 7.80 (dd, J=7.9, 1.6 Hz, 1H), 7.75 (m, 1H), 7.64 (m, 1H), 7.34 (d, J=7.6 Hz, 1H), 7.23 (d, J=7.9 Hz, 1H), 2.02 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791142B2
Source datasetuspto-grants-2014_07
ORD IDord-1aa97d9db37e464cbe93d5248e65c200
Source noteuspto-grants-2014_07