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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516109Generated: October 26, 2026

Water → 6-Nitro-4-(2-(4-tert-butylphenyl)ethoxy)quinazoline

https://huagongshe.com/reaction/1516109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactantp-tert-Butylphenethyl alcoholHCID 79410—
Reactant4-Chloro-6-nitroquinazolineHCID 11356257—
SolventTetrahydrofuranHCID 8028—
Product6-Nitro-4-(2-(4-tert-butylphenyl)ethoxy)quinazolineHCID 59678659—

Reaction Steps

2-(4-tert-butylphenyl)ethanol (1.0 g, 5.59 mmol) is dissolved in dry tetrahydrofuran (7 ml) and to it is added sodium hydride (48.5 mg, 2.02 mmol). The resulting solution is stirred at room temperature for 30 minutes after which 6-Nitro-4-chloroquinazoline (1.17 g, 5.6 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 numberUS08226929B2
Source datasetuspto-grants-2012_07
ORD IDord-66994f89b43541d8bfc3f1bb7cef1177
Source noteuspto-grants-2012_07