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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274143Generated: November 1, 2026

4-Methoxybenzyl alcohol → 7-Bromo-4-(4-methoxybenzyloxy)quinazoline

https://huagongshe.com/reaction/2274143

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl alcoholHCID 7738—
ReactantSodium hydrideHCID 24758—
Reactant7-Bromo-4-chloroquinazolineHCID 16780855—
SolventTolueneHCID 1140—
Product7-Bromo-4-(4-methoxybenzyloxy)quinazolineHCID 6740198734.5%

Reaction Steps

226.0 g (01.64 mol) of 4-methoxybenzyl alcohol in 0.5 l of toluene were added dropwise to a suspension of 80.0 g (2.0 mol) of sodium hydride [60% in paraffin oil] in 3.0 l of toluene between 15° C. and 20° C. The mixture was subsequently stirred at room temperature for a further 1 h. 165.9 g (1.64 mol) of 7-bromo-4-chloroquinazoline were then added in portions, and the reaction mixture was stirred for 48 h. Conventional work-up gave 194.8 g of 7-bromo-4-(4-methoxybenzyloxy)quinazoline as solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126952B2
Source datasetuspto-grants-2015_09
ORD IDord-ac47c607a0f84fa3a0640f5458d650c9
Source noteuspto-grants-2015_09