Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516113Generated: October 30, 2026

Tetrabutylammonium Fluoride → 1-Hydroxy-2-tetrahydropyranyloxy-2-(4-tert-butylphenyl)ethane

https://huagongshe.com/reaction/1516113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant1-Tert-butyldimethylsilyloxy-2-tetrahydropyranyloxy-2-(4-tertbutylphenyl) ethaneHCID 59678640—
SolventWaterHCID 962—
Product1-Hydroxy-2-tetrahydropyranyloxy-2-(4-tert-butylphenyl)ethaneHCID 59678708—

Reaction Steps

To 1-tert-butyldimethylsilyloxy-2-tetrahydropyranyloxy-2-(4-tertbutylphenyl)ethane (0.4 g, 1.01 mmol) is added tetrabutylammonium fluoride solution (1M TBAF in THF, 5 ml, 5.0 mmol). The solution is stirred for 2 hours after which water is added to the reaction and this is extracted in ethyl acetate. The organic layer is then washed with water, dried and concentrated. The residue obtained is purified by flash chromatography (silica gel; ethyl acetate/hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08226929B2
Source datasetuspto-grants-2012_07
ORD IDord-1dac8eb011824590be2a021bf671727a
Source noteuspto-grants-2012_07