Reacción #2045078

Ecuación de reacción

dibenzo[b,d]thiophen-4-yl lithium

m-bromophenyl lithium

n-butyllithium

hexane

1,3-dibromobenzene

m-bromophenyl lithium

dichlorodiphenylsilane

→

(3-bromophenyl)(dibenzo[b,d]thiophen-4-yl)diphenylsilane

Rendimiento 31.0%

Disolventes

ether

ether

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroThe resultant reaction solution
2. 2
   Otroprepared
3. 3
   workup.ADDITIONabove was introduced dropwise
4. 4
   OtroIt was quenched with water
5. 5
   Extracciónextracted with ether
6. 6
   Secadodried over Na2SO4
7. 7
   OtroUpon evaporation of the solvent
8. 8
   Otrothe residue was purified by column chromatography on silica gel with hexane/DCM (9/1

Procedimiento

In another flask was prepared a solution of m-bromophenyl lithium by addition of n-butyllithium solution in hexane (2.5 M, 9.48 mL, 23.70 mmol) into a solution of 1,3-dibromobenzene (2.56 mL, 21.20 mmol) in ether (70 mL) at −78° C. followed by stirring at this temperature for 3.5 h. This m-bromophenyl lithium solution was added dropwise into a solution of dichlorodiphenylsilane (4.88 mL, 23.70 mmol) in ether (70 mL) at −78° C. The resultant reaction solution was stirred at this temperature for 2 h before the dibenzo[b,d]thiophen-4-yl lithium solution prepared above was introduced dropwise. The resultant solution was allowed to slowly warm to room temperature overnight. It was quenched with water, extracted with ether and dried over Na2SO4. Upon evaporation of the solvent, the residue was purified by column chromatography on silica gel with hexane/DCM (9/1, v/v) as eluent to yield (3-bromophenyl)(dibenzo[b,d]thiophen-4-yl)diphenylsilane as a white powder (3.84 g, 31%).

Fuente