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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042685Generated: October 25, 2026

Ethanol → 3-(2-Nitro-4-(trifluoromethyl)phenyl)pyridine

https://huagongshe.com/reaction/1042685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-5-(trifluoromethyl)benzenamineHCID 67989—
Reactant3-Pyridinylboronic acidHCID 2734378—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product3-(2-Nitro-4-(trifluoromethyl)phenyl)pyridineHCID 46316762—

Reaction Steps

A mixture of pyridin-3-ylboronic acid (0.99 g, 8.1 mmol), 2-bromo-5-(trifluoromethyl)benzenamine (1.2 ml, 8.1 mmol), tetrakis(triphenylphosphine)palladium (0.28 g, 0.24 mmol), sodium carbonate (2.0 M solution in water, 8.0 ml, 16 mmol), 4 ml ethanol, and 20 ml toluene was heated to 90° C. under nitrogen with a water-cooled reflux condenser. After 12 h, mixture was cooled to ambient temperature, and was partitioned between EtOAc and 1N NaOH. The organic layer was washed once with brine, dried with Na2SO4, filtered, and concentrated to give a brown oil, which was further purified by silica gel chromatography (EtOAc/hexanes) to give the desired product as a waxy orange solid. MS (m/z): 269.0 (M+H)−. Calc'd for C12H7F3N2O2: 268.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557996B2
Source datasetuspto-grants-2013_10
ORD IDord-8939bd5cab6444898f34cf7b2157f512
Source noteuspto-grants-2013_10