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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392856Generated: October 30, 2026

Benzyl Alcohol → 2,4-Bisbenzyloxy-6-methoxyquinazoline

https://huagongshe.com/reaction/2392856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2,4-Dichloro-6-methoxyquinazolineHCID 9991397—
SolventTetrahydrofuranHCID 8028—
Product2,4-Bisbenzyloxy-6-methoxyquinazolineHCID 1879674695%

Reaction Steps

3 ml of benzyl alcohol was dissolved in 50 ml of tetrahydrofuran, followed by the addition of 1.0 g of sodium hydride. The obtained mixture was stirred at 40° to 50° C. for 30 minutes, followed by the addition of 2.50 g (0.0109 mol) of 2,4-dichloro-6-methoxyquinazoline. The obtained mixture was heated under reflux for several hours, followed by the addition of water. The obtained mixture was extracted with chloroform and the organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was distilled under a reduced pressure to remove the solvent. The obtained crystalline residue was recrystallized from chloroform/n-hexane to give 3.84 g of the title compound as a yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05801180
Source datasetuspto-grants-1998_09
ORD IDord-a4126e6fca3c40a8a50b47bbf7d4d0b1
Source noteuspto-grants-1998_09