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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 221111Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/221111

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
PatentnummerUS08202984B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-8fc2004b953e4e50b62929aa4fd2ac9a
Quellennotizuspto-grants-2012_06