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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237482Generated: October 28, 2026

Chlorotrimethylsilane → (4-Bromo-3,5-dimethylphenyl)trimethylsilane

https://huagongshe.com/reaction/237482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2,5-Dibromo-1,3-dimethylbenzeneHCID 2758047—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product(4-Bromo-3,5-dimethylphenyl)trimethylsilaneHCID 86697146—

Reaction Steps

A solution of 2,5-dibromo-1,3-dimethylbenzene (500 mg) in diethylether (3 mL) and tetrahydrofuran (2.5 mL) is cooled to −78° C. and treated dropwise with n-butyllithium (200 μL of a 10 M solution in n-hexane). The mixture is stirred for 1 hour and treated dropwise with chloro-trimethyl-silane (275 μL). After stirring for 2 hours the reaction is quenched by addition of saturated aqueous NH4Cl solution. The mixture is extracted with diethylether. The organic phase is dried (MgSO4) and concentrated. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 99:1→90:10) to give the title compound. Yield: 260 mg; Mass spectrum (ESI+): m/z=279 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642585B2
Source datasetuspto-grants-2014_02
ORD IDord-e10e31b119794a4995336d41bc01d136
Source noteuspto-grants-2014_02