HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185070Generated: November 1, 2026
Chlorodimethylphenylsilane → HCID 131723247, compound
https://huagongshe.com/reaction/2185070
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorodimethylphenylsilane | HCID 13029 | — |
| Reactant | 1,2,3,4-Tetramethylcyclopentadiene | HCID 138163 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131723247 | HCID 131723247 | — |
Reaction Steps
30 ml (48 mmol) of n-butyllithium (1.6 M in hexane) were added dropwise at −78° C. to a solution of 5.4 g (44.2 mmol) of tetramethylcyclopentadiene in 90 ml of THF over the course of about 20 minutes. The mixture was then stirred at 25° C. for 24 hours. The solution was then cooled again to −78° C., 8.3 g (48.6 mmol) of chlorodimethylphenylsilane were added dropwise over the course of 15 minutes, and the mixture was stirred at 25° C. for 24 hours. The THF was then removed under reduced pressure, and the residue was taken up in 50 ml of pentane. The insoluble precipitate was filtered off and the pentane was removed under reduced pressure. The yellow liquid residue was distilled under a high vacuum. The product boils at 83 to 85° C. Characterization was carried out by means of 1H-NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399727B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-58d337e79f66424896fd45c24c0d7997 |
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| Source note | uspto-grants-2002_06 |
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