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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216844Generated: October 27, 2026

Tributylvinyltin → 3-(2-Pyridyl)-5-(3-cyano-5-vinylphenyl)-1,2,4-oxadiazole

https://huagongshe.com/reaction/2216844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
Reactant3-(2-Pyridyl)-5-(3-bromo-5-cyanophenyl)-1,2,4-oxadiazoleHCID 9880426—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Pyridyl)-5-(3-cyano-5-vinylphenyl)-1,2,4-oxadiazoleHCID 992164278.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 3-(2-pyridyl)-5-(3-bromo-5-cyanophenyl)-1,2,4-oxadiazole (1.005 g, 3.21 mmol) and Pd(PPh3)4 (369 mg, 0.32 mmol) in tetrahydrofuran (10 mL) was treated with vinyl tributyl tin (0.985 mL, 3.36 mmol). The reaction mixture was heated in a sealed tube at 85° C. for 18 hours. After cooling, the mixture was diluted with dichloromethane and water. The organic layer was dried by filtration through an EX-TUBE. Silica gel chromatography afforded 691 mg (78%) of 3-(pyrid-2-yl)-5-(3-cyano-5-vinylphenyl)-1,2,4-oxadiazole: 1H-NMR (CDCl3), δ (ppm): □□□□□□ (s, 1H), 8.52 (s, 1H), 8.43 (s, 1H), 8.23 (d, 1H), 7.90 (m, 2H), 7.48 (m, 1H), 6.78 (dd, 1H), 5.98 (d, 1H), 5.55 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112595B2
Source datasetuspto-grants-2006_09
ORD IDord-d6034b239b5745e7ad8b4408335a7d31
Source noteuspto-grants-2006_09