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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528076Generated: October 30, 2026

Benzyl Bromide → 1-benzyl-3-chloro-5-methoxypyridazin-4(1H)-one

https://huagongshe.com/reaction/1528076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178493809HCID 178493809—
CatalystTetrabutylammonium IodideHCID 67553—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-benzyl-3-chloro-5-methoxypyridazin-4(1H)-oneHCID 86686560126.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Chloro-5-methoxypyridazin-4-ol (10.0 g) was dissolved in DMF (300 mL), sodium hydride (3.26 g, 55 wt %) and tetrabutylammonium iodide (4.60 g) were added thereto at 0° C., and the mixture was stirred at the same temperature for 10 min. To the reaction mixture was added benzyl bromide (12.3 g) at 0° C., and the mixture was stirred at room temperature for 20 hr. The reaction mixture was diluted with water, and the mixture was extracted with dichloromethane. The extract was washed with water and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was recrystallized from ethyl acetate/hexane to give the title compound (19.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090586B2
Source datasetuspto-grants-2015_07
ORD IDord-95080da3061d4b09a4330cdf51926902
Source noteuspto-grants-2015_07