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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440758Generated: October 30, 2026

Tributyltin Chloride → 2-(Tributylstannyl)-1,3-thiazole

https://huagongshe.com/reaction/440758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant2-BromothiazoleHCID 76430—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(Tributylstannyl)-1,3-thiazoleHCID 276325951.3%

Reaction Steps

To a solution of 10.0 g of 2-bromothiazole under nitrogen in 50 ml of tetrahydrofuran while cooling in a dry ice-acetone bath is added dropwise 36.6 ml of a 1.6M solution of butyl lithium via syringe. Stirring is continued for 1 hour. To the reaction mixture is added dropwise 29.8 g of tributyltin chloride in 20 ml of tetrahydrofuran. Stirred 1 additional hour. The reaction mixture is quenched with 20 ml of water and 50 ml additional water is added. After stirring for 20 minutes the reaction mixture is extracted with chloroform (3×60 ml). The organic layer is dried (Na2SO4) and evaporated in vacuo to give 11.7 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521173
Source datasetuspto-grants-1996_05
ORD IDord-a6ca1ec6dfb44af5aba1384ff2a9c0ef
Source noteuspto-grants-1996_05