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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantHexaneHCID 8058—
Reactant1-(Cyclopentadienyl)-1(3,6-di-tert-butylfluorenyl)diphenylmethaneHCID 131725132—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Trimethylsilylcyclopentadienyl)-1-(3,6-di-tert-butylfluorenyl)diphenylmethaneHCID 13172513382.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939928B1
Source datasetuspto-grants-2005_09
ORD IDord-678cefb0c2ff48c88212ab84bad6c3ed
Source noteuspto-grants-2005_09