Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281318Generated: November 2, 2026

Dichloromethane → 5-Ethenyl-2-(tetrazol-1-yl)pyridine

https://huagongshe.com/reaction/2281318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant5-Bromo-2-(tetrazol-1-yl)pyridineHCID 4136542—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-Ethenyl-2-(tetrazol-1-yl)pyridineHCID 89545188—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirring solution of 5-bromo-2-(1H-tetrazol-1-yl)pyridine (1.0 g, 4.42 mmol), in EtOH (70 mL) were added bis[(diphenylphosphino)ferrocene]dichloropalladium(II), complex with dichloromethane (0.361 g, 0.442 mmol), potassium vinyl trifluoroborate (1.18 g, 8.85 mmol, 2 equiv.), triethylamine (1.23 mL, 8.85 mmol, 2 equiv), and water (0.5 mL). The reaction mixture was heated to reflux (90° C., oil bath). Upon completion as determined by reverse phase HPLC-MS (1-2 h) and TLC (eluent: 10% ethyl acetate in hexanes), the reaction was cooled to room temperature, and then was diluted with water and extracted with EtOAc. The combined organic layers were washed with brine and dried over MgSO4. The extracts were concentrated and chromatographed over a column of SiO2 (0-20% EtOAc/hexanes as eluent). Evaporation of the solvent yielded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139585B2
Source datasetuspto-grants-2015_09
ORD IDord-9d2ea2b837d646d497c30a2e4526045f
Source noteuspto-grants-2015_09