Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428732Generated: October 31, 2026

Sodium Carbonate → 2-m-Tolyl-6-(trifluoromethyl)nicotinonitrile

https://huagongshe.com/reaction/1428732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-Tolylboronic acidHCID 2733950—
Reactant2-Chloro-6-(trifluoromethyl)nicotinonitrileHCID 2778413—
ReactantCyclohexane ethylacetateHCID 21867204—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-m-Tolyl-6-(trifluoromethyl)nicotinonitrileHCID 8668021549%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Chloro-6-(trifluoromethyl)nicotinonitrile (3 g, 14.56 mmol) was dissolved in toluene (70 mL) and ethanol (14 mL). m-tolylboronic acid (2.969 g, 21.814 mmol), aqueous sodium carbonate solution (2 M, 14 mL) and Pd(PPh3)4 (1.684 g, 1.456 mmol) were added. The mixture was flushed with nitrogen and stirred under microwave conditions (7 bar) at 100° C. for 2 h. The concentrated reaction mixture was cooled, diluted with ethyl acetate (200 mL), passed through celite (cyclohexane/ethyl acetate 9:1, 2×1 L) and concentrated in vacuo to afford 2-m-tolyl-6-(trifluoromethyl)nicotinonitrile (1.87 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937092B2
Source datasetuspto-grants-2015_01
ORD IDord-6f30511677c749ccbacfa832fd2b2618
Source noteuspto-grants-2015_01