Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212319Generated: November 2, 2026

Imidazole → tert-Butyl-(3,5-dibromobenzyloxy)diphenylsilane

https://huagongshe.com/reaction/2212319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant(3,5-Dibromophenyl)methanolHCID 7009423—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl-(3,5-dibromobenzyloxy)diphenylsilaneHCID 2196457194.4%

Reaction Steps

With stirring, imidazole (1.1 g, 16.0 mmol) is added to a solution of 3,5-dibromobenzyl alcohol (2.8 g, 10.5 mmol) in absolute DMF (20 ml), and the mixture is cooled to 0° C. tert-Butyldiphenylsilyl chloride (3.3 ml, 17.8 mmol) is added dropwise to the reaction solution, which is then stirred at 0° C. for 2 h. The mixture is then warmed to RT and stirred for another 2 h. The reaction mixture is diluted with ethyl acetate (20 ml) and extracted with a semisaturated aqueous NH4Cl solution (20 ml). The organic phase is dried over MgSO4, filtered off and concentrated under reduced pressure. Further purification is carried out by chromatography [PE/EA (99:1)] on a silica gel column. This gives the title compound (5.0 g) as a colorless solid. TLC, silica gel (glass plates), [petroleum ether/ethyl acetate (99:1)], Rf=0.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101911B2
Source datasetuspto-grants-2006_09
ORD IDord-b61e584ea3d64e6aaebcf1e04f10c912
Source noteuspto-grants-2006_09