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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360364Generated: November 3, 2026

Benzoyl Peroxide → 4-(Bromomethyl)-6,7-dimethoxyquinazoline

https://huagongshe.com/reaction/1360364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant6,7-Dimethoxy-4-methylquinazolineHCID 4319422—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
Product4-(Bromomethyl)-6,7-dimethoxyquinazolineHCID 59805849—

Reaction Steps

4-Methyl-6,7-dimethoxyquinazoline (D-1) (3.43 g, 14.7 mMol), N-bromosuccinimide (NBS) (2.64 g, 14.7 mMol) and benzoyl peroxide (BPO) (500 mg) were heated under reflux in 200 mL of carbon tetrachloride with irradiation by a 200 W sun lamp for 5 h. The reaction mixture was cooled to room temperature, diluted with dichloromethane and extracted twice with water. The combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. Flash chromatography on silica gel, eluting with hexanes/ethyl acetate gave 4-bromomethyl-6,7-dimethoxyquinazoline (E-1) as a pinkish solid, 1.39 g; 1H NMR (CDCl3, 300 MHz) 9.07 (s, 1H), 7.34 (s, 1H), 7.30 (s, 1H), 4.85 (s, 2H), 4.06 (s, 6H) ppm; 13C NMR (CDCl3, 75 MHz) 161.22, 156.32, 153.45, 150.72, 149.22, 118.85, 107.47, 101.78, 56.84, 56.70, 30.13; MS (ES) 283/285 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879856B2
Source datasetuspto-grants-2011_02
ORD IDord-684545d2efd046e2a4e575bd5c8be7e1
Source noteuspto-grants-2011_02