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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535700Generated: October 30, 2026

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

https://huagongshe.com/reaction/535700

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 numberUS08859536B2
Source datasetuspto-grants-2014_10
ORD IDord-c76b483e73224ae8beff4fbf424b796d
Source noteuspto-grants-2014_10