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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222218Generated: October 30, 2026

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

https://huagongshe.com/reaction/222218

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

Separately, 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 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 sodium chloride aqueous 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. 1, Step 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207189B2
Source datasetuspto-grants-2012_06
ORD IDord-aa93aa979e69492f86cde83da250a7da
Source noteuspto-grants-2012_06