Reaktion #80920
ord-40fd263cdcac48d5b00ae15c757d6318
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1TemperaturThe reaction mixture temperature was maintained at -85° C. to -80° C. throughout the addition
- 2workup.ADDITIONUpon completion of addition
- 3workup.ADDITIONUpon completion of addition
- 4Temperaturto warm gradually to ambient temperature
- 5SonstigeThe reaction was quenched with an aqueous solution saturated with ammonium chloride
- 6Extraktionthe reaction mixture was extracted with three 150 mL portions of diethyl ether
- 7TrocknenThe combined extracts were dried with magnesium sulfate
- 8Filtrationfiltered
- 9EinengenThe filtrate was concentrated under reduced pressure
Vorschrift
A stirred solution of 5.1 mL (0.046 mole) of 2-bromo-5-chlorothiophene in 200 mL of tetrahydrofuran was cooled to -85° C., and 19.7 mL (0.049 mole) of n-butyllithium (0.049 mole-2.5M in hexanes) was added dropwise during a 15 minute period. The reaction mixture temperature was maintained at -85° C. to -80° C. throughout the addition. Upon completion of addition, the reaction mixture temperature was maintained at about -80° C. for one hour. After this time, a solution of 12.5 mL (0.046 mole) of tributyltin chloride in 50 mL of tetrahydrofuran was added to the cold reaction mixture during a 10 minute period. Upon completion of addition, the reaction mixture was stirred at -80° C. for one hour, then it was allowed to warm gradually to ambient temperature. The reaction was quenched with an aqueous solution saturated with ammonium chloride, and then the reaction mixture was extracted with three 150 mL portions of diethyl ether. The combined extracts were dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 18.4 grams of (5-chlorothien-2-yl)tributyl tin. The NMR spectrum was consistent with the proposed structure.