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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755677Generated: November 2, 2026

Benzene → (2-Bromoethoxy)-tert-butyldimethylsilane

https://huagongshe.com/reaction/1755677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantImidazoleHCID 795—
Reactant2-BromoethanolHCID 10898—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDimethylformamideHCID 6228—
Product(2-Bromoethoxy)-tert-butyldimethylsilaneHCID 360806794%

Reaction Steps

2 g of ethylene bromohydrin and 2.4 g of imidazole were dissolved in 40 ml of N,N-dimethylformamide, to which 2.65 g of t-butyldimethylsilyl chloride were added at room temperature. After completion of the reaction, benzene was added, followed by washing with water and a sodium hydrogencarbonate aqueous solution and drying with anhydrous magnesium sulfate. This was filtered and the solvent was distilled off, thereby obtaining 3.60 g of the captioned compound (yield 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05438045
Source datasetuspto-grants-1995_08
ORD IDord-35e93e8fc41845ce98d397acfd3c51f3
Source noteuspto-grants-1995_08