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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21909Generated: October 25, 2026

Tetrahydrofuran → Stannane, tributyl-3-furanyl-

https://huagongshe.com/reaction/21909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTributyltin ChlorideHCID 15096—
Reactant3-BromofuranHCID 89164—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductStannane, tributyl-3-furanyl-HCID 11760097—

Reaction Conditions

Temperature-60 °C

Reaction Steps

69.5 ml of a 1.6 molar solution of n-butyllithium in hexane are mixed with 60 ml of absolute tetrahydrofuran. The mixture is cooled to -60° C. and 10 ml of 3-bromofuran are added dropwise at such a rate that the internal temperature does not exceed -50° C.. When the addition is complete, the whole is stirred for 15 minutes at -60° C. and then 33.2 ml of tributyltin chloride are added dropwise, during the course of which the internal temperature is not allowed to exceed -50° C.. When the addition is complete, the reaction solution is allowed to come to -10° C. and is then stirred for one hour at that temperature. The solution is then carefully quenched with water. The aqueous phase is extracted with ethyl acetate. The organic phase is washed with saturated sodium chloride solution and dried over sodium sulphate. It is filtered off and the solvent is removed in vacuo. The crude product obtained is purified by distillation in a high vacuum. 30.14 g of (3-furanyl)tributylstannane are obtained in the form of a light-yellow oil (boiling point=100°-104° C. at 0.09 torr).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426102
Source datasetuspto-grants-1995_06
ORD IDord-6be063efd36f4a1c8d76b87968f64262
Source noteuspto-grants-1995_06