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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213327Generated: October 30, 2026

Ethyl Acetate → HCID 10149245, compound

https://huagongshe.com/reaction/2213327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Reactant2-(3-BROMO-1H-1,2,4-TRIAZOL-1-YL)PYRIDINEHCID 11206876—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 10149245HCID 10149245—

Reaction Conditions

Temperature90 °C

Reaction Steps

2-(3-Bromo-1H-1,2,4-triazol-1-yl)pyridine (0.25 g, 1.12 mmol) and 3-chlorophenylboronic acid (0.35 g, 2.23 mmol) were dissolved in toluene (20 mL) and methanol (2 mL), then deoxygenated via argon bubbling for 10 min. Potassium carbonate (0.23 g, 1.6 mmol) and tetrakis(triphenylphosphine)palladium (129 mg, 0.11 mmol) were added to this stirred solution. The reaction container was fitted with a reflux condenser and stirred at 90° C. for 16 h, after which time it was cooled to ambient temperature and poured into a separatory funnel containing EtOAc (100 mL). The EtOAc solution was washed with H2O (2×100 mL), then brine (100 mL) and the organic phase was dried (MgSO4), filtered and concentrated in vacuo. The resulting crude residue was chromatographed on silica gel eluting with hexanes:EtOAc (8:2) to afford 2-[3-(3-chlorophenyl)-1H-1,2,4-triazol-1-yl]pyridine as a white powder which was dissolved in dichloromethane (10 mL) and precipitated as the hydrochloride salt (M.p.=125–128° C.) upon treatment with 1M HCl in diethyl ether (1 mL).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105548B2
Source datasetuspto-grants-2006_09
ORD IDord-1f8cf5f0cd4c4923b1660080ed5866ea
Source noteuspto-grants-2006_09