HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729002Generated: October 30, 2026
Chlorotrimethylsilane → 2,2'-Dilithiobiphenyl
https://huagongshe.com/reaction/1729002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Calcium | HCID 5460341 | — |
| Reactant | Calcium iodide | HCID 5462722 | — |
| Reactant | Lithium anthracen-1-ide | HCID 15303778 | — |
| Product | 2,2'-Dilithiobiphenyl | HCID 12532846 | — |
Reaction Steps
Preformed lithium anthracenide was reacted with calcium iodide to prepare asoluble calcium species. This calcium species was added to chloromethylatedpolystyrene (DF=0.11) and stirred for 24 hours at room temperature. The corresponding calcium-substituted reagent was then reacted with chlorotrimethylsilane at room temperature to yield the silylated product; however, the yield was not optimized and was lower than the yield obtainedfrom preformed lithium biphenylide (Table III, entry 4). Reaction of the calcium species with chloromethylated polystyrene at 0° C. for 6 hours resulted in a 100% loss of chlorine from the polymer. Subsequent reaction with benzaldehyde gave the corresponding secondary alcohol in 80%yield, compared to the 100% yield when calcium biphenylide was used (Table III, entry 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05330687 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-be13d9bdd0a24fbaac738f1cc510f859 |
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| Source note | uspto-grants-1994_07 |
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