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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576584Generated: October 31, 2026

Benzyl Bromide → 3-benzyl-6-bromoquinazolin-4(3H)-one

https://huagongshe.com/reaction/576584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant6-bromoquinazolin-4-olHCID 135444905—
SolventDimethylformamideHCID 6228—
Product3-benzyl-6-bromoquinazolin-4(3H)-oneHCID 118750757.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

Benzyl bromide (0.264 mL, 2.22 mmol) was added to a solution of 6-bromoquinazolin-4(3H)-one (0.5 g, 2.22 mmol) and NaH (0.08 g, 3.33 mmol) in DMF (5 mL) at 0° C. The reaction mixture was heated to 80° C. for 4 h. The reaction mixture was partitioned between ethyl acetate and water. Organic layer was separated, washed with brine, dried over sodium sulphate, filtered and concentrated in vacuo to afford title compound (0.4 g, 48.1%) as pale yellow solid. 1H NMR (400 MHz, CDCl3): δ 8.46 (d, J=1.6 Hz, 1H), 8.09 (s, 1H), 7.83 (dd, J1=2.0 Hz, J2=8.8 Hz, 1H), 7.57 (d, J=8.4 Hz, 1H), 7.4-7.2 (m, 5H), 5.2 (s, 2H); ESI-MS m/z=315 (M+H)+; LCMS purity: 84.2%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040517B2
Source datasetuspto-grants-2015_05
ORD IDord-24e00efc82e24fb5a65e4025d99c2b86
Source noteuspto-grants-2015_05