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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055557Generated: October 26, 2026

2-Bromoethanol → 3-(2-hydroxyethyl)-6,7-dimethoxy-4(3H)-quinazolinone

https://huagongshe.com/reaction/2055557

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
Reactant4(1H)-QuinazolinoneHCID 135408753—
Reactant6,7-Dimethoxy-3H-quinazolin-4-oneHCID 135495016—
SolventAcetoneHCID 180—
Product3-(2-hydroxyethyl)-6,7-dimethoxy-4(3H)-quinazolinoneHCID 22326622—

Reaction Steps

3-(2-hydroxyethyl)-6,7-dimethoxy-4(3H)-quinazolinone was prepared from 6,7-dimethoxy-4(3H)-quinazolinone (3 g, 14.6 mmol). The quinazolinone was combined with 2-bromoethanol (1.14 mL, 16 mmol), an excess of potassium carbonate (10 g) and heated at reflux in 200 mL acetone. The salts were filtered off and the reaction mixture was concentrated. The residue was dissolved in chloroform and washed with water. The organic layer was dried over Na2SO4, filtered and concentrated, 1.39 g (38%); light brown powder; m.p. 130° C., MS: 250.9 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332506B2
Source datasetuspto-grants-2008_02
ORD IDord-e1655fcd948c4ae0adf69465d94a03c8
Source noteuspto-grants-2008_02