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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810608Generated: October 29, 2026

Chlorodimethylsilane → AC1LBHMA

https://huagongshe.com/reaction/1810608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodimethylsilaneHCID 66108—
ReactantSilane, (chloromethyl)trimethyl-HCID 75361—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductSilane, (chloromethyl)trimethyl-HCID 75361—
ProductAC1LBHMAHCID 582874177.6%

Reaction Steps

The Grignard reagent of trimethylchloromethylsilane was prepared by reacting trimethylchloromethylsilane (12.3 grams, 0.1 mole) with magnesium chips (2.88 grams, 0.12 mole) in tetrahydrofuran (50 milliliters. The Grignard reagent was then added dropwise into dimethylchlorosilane (9.46 grams 0.1 mole), which was dissolved in tetrahydrofuran (50 milliliters). The mixture was stirred at room temperature overnight, quenched with hydrochloric acid solution (20 milliliters), and extracted with diethyl ether (100 milliliters). The organic layer was washed with distilled water three times and dried with anhydrous sodium sulfate. The mixture was purified by distillation at 118-119° C. to yield (trimethylsilylmethyl)dimethylsilane product (13.0 grams, 89% yield) as a clear, colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362124B2
Source datasetuspto-grants-2013_01
ORD IDord-5eb02a3b6f6f47149071dc67a6a0da56
Source noteuspto-grants-2013_01