HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495754Generated: October 29, 2026
Chlorotrimethylsilane → 1-(3-Trimethylsilylcyclopentadienyl)-1-(3,6-di-tert-butylfluorenyl)diphenylmethane
https://huagongshe.com/reaction/495754
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1-(Cyclopentadienyl)-1(3,6-di-tert-butylfluorenyl)diphenylmethane | HCID 131725132 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-Trimethylsilylcyclopentadienyl)-1-(3,6-di-tert-butylfluorenyl)diphenylmethane | HCID 131725133 | 82.2% |
Reaction Steps
To a solution of 0.45 g (0.88 mmol) of 1-(cyclopentadienyl)-1-(3,6-di-tert-butylfluorenyl)diphenylmethane in 30 ml of THF, 0.54 ml (0.97 mmol) of a hexane solution of n butyllithium was dropwise added in a nitrogen atmosphere with ice cooling, followed by stirring at room temperature for 16 hours. After the resulting solution was cooled to −78° C., a solution of 0.22 ml (1.76 mmol) of chlorotrimethylsilane in 10 ml of THF was slowly added, followed by stirring at room temperature for 6 hours. To the reaction solution, 20 ml of water was added to terminate the reaction. The resulting solution was subjected to extraction with diethyl ether, then dried over anhydrous magnesium sulfate and vacuum evaporated to dryness to obtain a yellow solid. The solid was washed with a small amount of methanol and dried under reduced pressure to obtain 0.42 g of an opaque white solid (yield: 81.8%). The analyzed values are given below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06939928B1 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-678cefb0c2ff48c88212ab84bad6c3ed |
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| Source note | uspto-grants-2005_09 |
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