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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichlorodiphenylsilane | HCID 6627 | — |
| Reactant | 1,3-Dibromobenzene | HCID 7927 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | C12H7LiS | HCID 178506665 | — |
| Reactant | HCID 178506674 | HCID 178506674 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3-Bromophenyl)(dibenzo[b,d]thiophen-4-yl)diphenylsilane | HCID 86676048 | 31% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08409729B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-0ec4363bc7ac4eaba7772917abab45fe |
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| Source note | uspto-grants-2013_04 |
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