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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392876Generated: November 1, 2026

Tetrabutylammonium Fluoride → 4-(2-(4-(4-Hydroxybutyl)phenyl)ethoxy)quinazoline

https://huagongshe.com/reaction/1392876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-(2-(4-(4-Tert-butyldimethylsilyloxybutyl)phenyl)ethoxy)quinazolineHCID 59678692—
SolventWaterHCID 962—
Product4-(2-(4-(4-Hydroxybutyl)phenyl)ethoxy)quinazolineHCID 44441989—

Reaction Steps

To 4-(2-(4-(4-tert-butyldimethylsilyloxybutyl) phenyl) ethoxy) quinazoline (0.4 g, 0.916 mmol) is added tetrabutylammonium fluoride solution (1M TBAF in THF, 4.58 ml, 4.58 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 numberUS07344702B2
Source datasetuspto-grants-2008_03
ORD IDord-761e388a9cf243e2ab3c1962eb3ef14d
Source noteuspto-grants-2008_03