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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747799Generated: October 30, 2026

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

https://huagongshe.com/reaction/1747799

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 Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150588B2
Source datasetuspto-grants-2015_10
ORD IDord-24469635a0c54183a29e172b71aa934f
Source noteuspto-grants-2015_10