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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392621Generated: October 30, 2026

Sodium Carbonate → 4-Chloro-6-(2,6-diethylphenyl)-2-trifluoromethyl-nicotinic acid methyl ester

https://huagongshe.com/reaction/1392621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(2,6-Diethylphenyl)boronic acidHCID 18437832—
Reactant4,6-Dichloro-2-trifluoromethyl-nicotinic acid methyl esterHCID 59678207—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product4-Chloro-6-(2,6-diethylphenyl)-2-trifluoromethyl-nicotinic acid methyl esterHCID 59678357—

Reaction Steps

A mixture of 4,6-dichloro-2-trifluoromethyl-nicotinic acid methyl ester (1.0 g, 3.7 mmol), 2,6-diethyl-phenyl boronic acid (0.78 g, 4.4 mmol), sodium carbonate (2 M aqueous solution, 4.4 mL, 8.8 mmol), and Pd(PPh3)4 (206 mg, 0.18 mmol) is refluxed in toluene for 48 hours and then cooled to room temperature. The organic layer is separated and the aqueous layer is extracted with ethyl acetate (2×50 mL). The combined organic layers are dried and the solvent removed. The crude product is purified by flash column (hexanes/ethyl acetate 8:1) to give 4-chloro-6-(2,6-diethyl-phenyl)-2-trifluoromethyl-nicotinic acid methyl ester as a white solid. 1H NMR: (CDCl3) 7.58 (s, 1H), 7.25 (t, 1H), 7.20 (d, 2H), 4.02 (s, 2.28 (q, 4H), 1.04 (t, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342115B2
Source datasetuspto-grants-2008_03
ORD IDord-922bd46e0ba545a8835347a55f43918d
Source noteuspto-grants-2008_03