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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270248Generated: October 31, 2026

Benzyl Bromide → HCID 22632888, compound

https://huagongshe.com/reaction/2270248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 22632985HCID 22632985—
SolventDimethylformamideHCID 6228—
ProductHCID 22632888HCID 22632888107.9%

Reaction Steps

A solution of 3-allyloxy-6,7-difluoro-1H-quinazoline-2,4-dione (Example Z-3, 0.7 g, 2.8 mmol) in 20 mL of DMF was added to a suspension of sodium hydride (0.12 g, 3.0 mmol) in 15 mL of DMF and stirred for 30 minutes. Benzyl bromide (0.65 mL, 5.5 mmol) was added, and the mixture was stirred at 25° C. for 18 hours. The reaction was quenched with 1 mL of water and concentrated to an oil. The residue was dissolved in chloroform washed with water and brine and dried over magnesium sulfate. The solution was concentrated to give 1.04 g of the title compound as a solid, mp 130-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331538B1
Source datasetuspto-grants-2001_12
ORD IDord-38c8ce550c9d42209175bbb41035e8f4
Source noteuspto-grants-2001_12