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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265952Generated: October 26, 2026

Chlorotrimethylsilane → Trimethyl(M-tolyl)silane

https://huagongshe.com/reaction/1265952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1,2-DibromoethaneHCID 7839—
Reactant3-ChlorotolueneHCID 7931—
ReactantSodium BicarbonateHCID 516892—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductTrimethyl(M-tolyl)silaneHCID 1086668492%

Reaction Steps

A solution of m-chlorotoluene (12.66 g, 0.100 mol) and 1,2-dibromoethane (0.5 ml) in THF (20 ml) was added to magnesium turnings (2.67 g, 0.110 mol). The mixture was heated under reflux for 4 h, after which the heating bath was removed and trimethylchlorosilane (11.08 g, 0.102 mol) was added so that gentle reflux was maintained. The mixture was stirred for another 0.5 h and 5% NaHCO3 (100 ml) was then added. The resulting mixture was extracted with CH2Cl2 (3×50 ml), the organic phase was washed with brine and dried (MgSO4). Filtration and evaporation provided 15.05g (92%) of 36 as a pale yellow liquid. Spectroscopic data were identical to those previously reported in the literature.40

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548042B2
Source datasetuspto-grants-2003_04
ORD IDord-bfe9f852ba984c97a54e5a941fac1ebb
Source noteuspto-grants-2003_04