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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079216Generated: October 30, 2026

Hydrochloric Acid → t-Butyl-(4-fluoro-3-methoxybenzyloxy)diphenylsilane

https://huagongshe.com/reaction/2079216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Reactant(4-Fluoro-3-methoxyphenyl)methanolHCID 593590—
Reactant4-{[(3-ethoxy-4-methoxyphenyl)-(5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]triazol-3-yl)methyl]amino}benzamidine acetateHCID 136366259—
SolventEthyl AcetateHCID 8857—
Productt-Butyl-(4-fluoro-3-methoxybenzyloxy)diphenylsilaneHCID 67097579—

Reaction Steps

After dissolving 9.17 g of (4-fluoro-3-methoxyphenyl)methanol [CAS No. 128495-45-4] in 100 ml of DMT, 5g of imidazole and 17g of t-butyl -chlorodiphenylsilane were added and the mixture was stirred overnight at room temperature. Next, 1N hydrochloric acid was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give t-butyl-(4-fluoro-3-methoxybenzyloxy)diphenylsilane as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928228B2
Source datasetuspto-grants-2011_04
ORD IDord-3571530c93cb4b3ca4c1cc3c21131d56
Source noteuspto-grants-2011_04