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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 550020Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/550020

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1-DibromoethaneHCID 11201—
EduktTributyltin ChlorideHCID 15096—
Edukt1-Bromo-4-ethylbenzeneHCID 15313—
EduktPotassium FluorideHCID 522689—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTributyl-(4-ethylphenyl)stannaneHCID 6004126792,9%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943788B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-b5edb5ae1c5e4f3a816d90afd537ab9f
Quellennotizuspto-grants-2011_05