Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440757Generated: October 30, 2026

2-Bromopyridine → 2-(Tributylstannyl)pyridine

https://huagongshe.com/reaction/440757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantTributyltin ChlorideHCID 15096—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(Tributylstannyl)pyridineHCID 60778491%

Reaction Steps

To a solution of 10.0 g of 2-bromo-pyridine under nitrogen in 100 ml of tetrahydrofuran while cooling in a dry ice-acetone bath is added dropwise 47.0 ml of a 1.6M solution of butyl lithium via syringe. Stirring is continued for 1 hour. To the reaction mixture is added dropwise 24.7 g of tributyltin chloride in 30 ml of tetrahydrofuran and stirred 1 additional hour. The reaction mixture is quenched with 20 ml of water and 100 ml additional water is added. After stirring for 20 minutes the reaction mixture is extracted with chloroform (3×100 ml). The organic layer is filtered through diatomaceous earth and the filtrate washed with saturated NaHCO3 and water. The organic layer is dried (Na2SO4) and evaporated in vacuo to give 21.2 g of the desired product. MS 379.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521173
Source datasetuspto-grants-1996_05
ORD IDord-b2a2d47e8de741758244be0e9d5e09e0
Source noteuspto-grants-1996_05