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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246533Generated: October 31, 2026

1,1-Dibromoethane → HCID 57659389, compound

https://huagongshe.com/reaction/2246533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DibromoethaneHCID 11201—
ReactantAllylchlorodimethylsilaneHCID 77646—
Reactant2-(2-Bromoethyl)-1,3-dioxolaneHCID 87776—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57659389HCID 57659389—

Reaction Steps

To a slurry of magnesium (2.43 g) in dry tetrahydrofuran (50 mL), few drops of dibromoethane (˜50 μL) was added under argon and stirred at room temperature for 10 min. The reaction mixture was cooled to 10° C. and 2-(2-bromoethyl)-1,3-dioxolane (10.9 g) was introduced dropwise during 10 min and allowed to stir at room temperature for 2 hours. The resulting reaction mixture was cooled to −10° C. and allyldimethylchlorosilane (6.73 g) was added dropwise during 10 min. and stirred over night at room temperature. Finally, the reaction content was quenched with aqueous NaHCO3 (15 mL) and extracted with ether (3×50 mL). The combined organic layer was dried and concentrated under mild vacuum to obtain the crude product, which was advanced to the next step without further purification (yield 9.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687496B2
Source datasetuspto-grants-2010_03
ORD IDord-7394fa015b1347c9a15e28d54897c96a
Source noteuspto-grants-2010_03