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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220130Generated: October 25, 2026

Tributyltin Chloride → 4-Tri-n-butylstannylfuran-2-carbonitrile

https://huagongshe.com/reaction/2220130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
Reactant4-Bromofuran-2-carbonitrileHCID 21986220—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product4-Tri-n-butylstannylfuran-2-carbonitrileHCID 6861524553%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium (1.6M, 3.7 mL, 5.93 mmol) was added to a solution of 4-bromofuran-2-carbonitrile (850 mg, 4.94 mmol) in anhydrous ether (15 mL) stirred at −78° C. under nitrogen. After 10 min, tri-n-butylstannyl chloride (1.61 g, 4.94 mmol) was added, then the reaction mixture was allowed to warm to room temperature, and stirred for another 1 h. The mixture was quenched, and washed with 1N sodium hydroxide, dried through MgSO4, and then the solvent was evaporated to give a brown oily residue. Purification by flash chromatography using a gradient of ammoniated methanol in chloroform gave the sub-title compound as a yellow oil (1.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417049B2
Source datasetuspto-grants-2008_08
ORD IDord-6310cf939366470baa4f36fbe280f5ee
Source noteuspto-grants-2008_08