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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060478Generated: October 26, 2026

Imidazole → 3,5-Dimethoxybenzyl tert-butyldiphenylsilyl ether

https://huagongshe.com/reaction/1060478

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), t-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-dimethoxy-1-[(t-butyldiphenylsilyloxy)methyl]benzene. ESMS: m/z 407 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521666B1
Source datasetuspto-grants-2003_02
ORD IDord-4841f5c4415d4c9b8f8776b2224e030b
Source noteuspto-grants-2003_02