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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24708Generated: October 23, 2026

Imidazole → 3,5-Dimethoxybenzyl tert-butyldiphenylsilyl ether

https://huagongshe.com/en/reaction/24708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant3,5-Dimethoxybenzyl alcoholHCID 69718—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
SolventDimethylformamideHCID 6228—
Product3,5-Dimethoxybenzyl tert-butyldiphenylsilyl etherHCID 2257188387.9%

Reaction Steps

A mixture of 3,5-dimethoxybenzyl alcohol (4.0 g), tert-butyl-diphenylsilyl chloride (6.54 g) and imidazole (3.28 g) in DMF (60 mL) was stirred at room temperature for 24 h. DMF was evaporated and the residue was purified by column chromatography (silica gel; eluent: hexane to hexane/EtOAc 20% ) to yield 8.5 g of 3,5-dimethoxybenzyl tert-butyldiphenylsilyl ether. ESMS: m/z 407 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855843B2
Source datasetuspto-grants-2005_02
ORD IDord-5a5ba54c17ac44b8bce09720bb95188c
Source noteuspto-grants-2005_02