Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751879Generated: October 28, 2026

Water → 4-(2-(4-(4-Tert-butyldimethylsilyloxybutyl)phenyl)ethoxy)quinazoline

https://huagongshe.com/reaction/1751879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-ChloroquinazolineHCID 78864—
Reactant2-[4-(4-{[tert-Butyl(dimethyl)silyl]oxy}butyl)phenyl]ethan-1-olHCID 59678712—
SolventTetrahydrofuranHCID 8028—
Product4-(2-(4-(4-Tert-butyldimethylsilyloxybutyl)phenyl)ethoxy)quinazolineHCID 59678692—

Reaction Steps

2-hydroxyethyl-4-(4-tert-butyldimethylsilyloxybutyl)benzene (0.3 g, 0.97 mmol) is dissolved in dry tetrahydrofuran and to it is added sodium hydride (24 mg, 1 mmol). The resulting solution is stirred at room temperature for 30 minutes after which 4-chloroquinazoline (0.164 g, 1 mmol) is added to the above solution. The solution is then stirred for 6 hours after which water is added to the mixture. The solution is then extracted in dichloromethane. The organic layer is washed, dried and then concentrated to yield the crude product which is purified by flash chromatography (silica gel; ethyl acetate/hexanes) to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09161997B2
Source datasetuspto-grants-2015_10
ORD IDord-1b425366d8ec483fbd47fcd9c8cae37f
Source noteuspto-grants-2015_10