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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242236Generated: November 1, 2026

Tetrahydrofuran → {4-[5-(4-Isobutylphenyl)-1,3,4-oxadiazol-2-yl]phenyl}methanol

https://huagongshe.com/reaction/2242236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-[4-({[Tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]-5-(4-isobutylphenyl)-1,3,4-oxadiazoleHCID 59204284—
SolventEthyl AcetateHCID 8857—
Product{4-[5-(4-Isobutylphenyl)-1,3,4-oxadiazol-2-yl]phenyl}methanolHCID 5920427688.5%

Reaction Steps

Tetrabutylammonium fluoride (1.0 M in THF, 2.0 mL) was added to a solution of 2-[4-({[tert-butyl(dimethyl)silyl]oxy}methyl)phenyl]-5-(4-isobutylphenyl)-1,3,4-oxadiazole (0.50 g, 1.18 mmol) and THF (10 mL) and stirred at room temperature for 16 hours. The reaction mixture was diluted with ethyl acetate (100 mL), washed with water and brine, dried (Na2SO4,), filtered and concentrated in vacuo to give the title compound (0.322 g, 88% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671043B2
Source datasetuspto-grants-2010_03
ORD IDord-b18b14a2adc740f8bcc93019f46efd5f
Source noteuspto-grants-2010_03