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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724498Generated: October 31, 2026

(2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane → (2-Dimethylamino-4,5-dimethylcyclopentadienyl)(2-allyloxy-3-tert-butyl-5-methylphenyl)dimethylsilane

https://huagongshe.com/reaction/724498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Allyloxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilaneHCID 21880918—
ReactantHCID 178506779HCID 178506779—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(2-Dimethylamino-4,5-dimethylcyclopentadienyl)(2-allyloxy-3-tert-butyl-5-methylphenyl)dimethylsilaneHCID 58747148102.7%

Reaction Steps

A solution of (2-allyloxy-3-tert-butyl-5-methylphenyl)dimethylchlorosilane (7.0 mmol) in toluene (12.1 mL) was added dropwise to a solution of 1-dimethylamino-3,4-dimethylcyclopentadienyllithium (7.0 mmol) in tetrahydrofuran (10.5 mL) and the mixture was stirred at room temperature for 6 hours. After the solvent was distilled off under reduced pressure, dehydrated pentane was added and a precipitated solid was filtered off. The filtrate was concentrated to obtain the title compound (2.86 g, 100%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141690B2
Source datasetuspto-grants-2006_11
ORD IDord-acdf963addc5423383edfa9cbf274e08
Source noteuspto-grants-2006_11