Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625849Generated: October 26, 2026

1,1-Dibromoethane → Tributyl-(4-ethylphenyl)stannane

https://huagongshe.com/reaction/1625849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DibromoethaneHCID 11201—
ReactantTributyltin ChlorideHCID 15096—
Reactant1-Bromo-4-ethylbenzeneHCID 15313—
ReactantPotassium FluorideHCID 522689—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductTributyl-(4-ethylphenyl)stannaneHCID 6004126792.9%

Reaction Steps

To a solution of magnesium (896 mg) in tetrahydrofuran (20 ml) was added dibromoethan (0.1 ml), and the mixture was stirred at room temperature for 15 minutes. Thereto was added dropwise a solution of 1-bromo-4-ethylbenzene (5.7 g) in tetrahydrofuran (20 ml), and subsequently, the mixture was stirred at room temperature for one hour. The reaction mixture was cooled to −78° C., and thereto was added dropwise tributyltin chloride (9.49 g). The mixture was stirred at the same temperature for 30 minutes, and then at room temperature for one hour. To the reaction mixture were added 10% aqueous potassium fluoride solution and ethyl acetate, and the mixture was stirred at room temperature for 30 minutes. Insoluble materials were filtered off. The organic layer of the filtrate was washed with water and brine successively, and dried over sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by alumina column chromatography (hexane) to give the desired tri-n-butyl(4-ethylphenyl)tin (10.7 g) as colorless oil. EI-Mass m/Z 337 (M-Bu).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-99bc2f8f412b49c5965786b6e664c47f
Source noteuspto-grants-2014_07