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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948878Generated: October 30, 2026

Imidazole → (2-Bromoethoxy)(tert-butyl)diphenylsilane

https://huagongshe.com/reaction/1948878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium ChlorideHCID 5234—
Reactant2-BromoethanolHCID 10898—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
SolventDimethylformamideHCID 6228—
Product(2-Bromoethoxy)(tert-butyl)diphenylsilaneHCID 1091544297%

Reaction Conditions

Temperature0 °C

Reaction Steps

2.50 g (corresponding to 20.0 mmol) of 2-bromoethanol and 2.72 g (corresponding to 40.0 mmol) of imidazole were dissolved in 10 mL of N,N-dimethylformamide (DMF), and cooled to 0° C. Then, 5.50 g (corresponding to 20.0 mmol) of t-butyldiphenylchlorosilane (TBDPSCl) was added thereto. After the reaction mixture was stirred at room temperature for 18 hours, a saturated aqueous sodium chloride solution was added, and extracted three times with ethyl acetate. The combined ethyl acetate layers were dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=10/1) to obtain 7.04 g (corresponding to 19.4 mmol) of 1-bromo-2-(t-butyldiphenylsiloxy)ethane (FIG. 7, Step 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399672B2
Source datasetuspto-grants-2013_03
ORD IDord-51680f4c419a4d82b1e708edff38ac69
Source noteuspto-grants-2013_03