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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289267Generated: October 31, 2026

Water → HCID 54565416, compound

https://huagongshe.com/reaction/1289267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1,2,3-TrimethylindeneHCID 588778—
ReactantHCID 178418306HCID 178418306—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54565416HCID 54565416—

Reaction Steps

1,2,3-Trimethylindene in an amount of 4.09 g (26 mmol) was dissolved in 100 mL of dried THF, and to the resultant solution was added dropwise, under ice-cooling 19 mL of a 1.7M solution of tert-butyllithium in pentane. After 2 hours of reaction at room temperature, the reaction product was incorporated under ice-cooling with 3.25 g (30 mmol, 3.8 mL) of trimethylchlorosilane (TMSCl) that had been subjected to simple distillation, was brought back to room temperature and was allowed to stand overnight. The yellow solution thus obtained was incorporated with 20 mL of water for quenching and THF was removed under reduced pressure. Then, the solution was extracted and separated with 300 mL of hexane, the organic phase thus obtained was dried with magnesium sulfate anhydride as the drying agent, the used drying agent was filtered away, and the volatile components were distilled away under reduced pressure. As the result, there was produced 1,2,3-trimethylindenyltrimethylsilane in the form of yellow oil in a yield of 4.27 g (18.5 mmol) and in a yield rate of 72%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747614
Source datasetuspto-grants-1998_05
ORD IDord-40a5d4a72e1a49af8ec50e432125ee9a
Source noteuspto-grants-1998_05