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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957896Generated: October 26, 2026

Dichlorodiphenylsilane → (3-Bromophenyl)(dibenzo[b,d]thiophen-4-yl)diphenylsilane

https://huagongshe.com/reaction/1957896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichlorodiphenylsilaneHCID 6627—
Reactant1,3-DibromobenzeneHCID 7927—
ReactantHexaneHCID 8058—
ReactantButyllithiumHCID 178418339—
ReactantC12H7LiSHCID 178506665—
ReactantHCID 178506674HCID 178506674—
SolventDiethyl EtherHCID 3283—
Product(3-Bromophenyl)(dibenzo[b,d]thiophen-4-yl)diphenylsilaneHCID 8667604831%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08409729B2
Source datasetuspto-grants-2013_04
ORD IDord-0ec4363bc7ac4eaba7772917abab45fe
Source noteuspto-grants-2013_04