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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333724Generated: October 30, 2026

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

https://huagongshe.com/reaction/333724

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 N,N-dimethylformamide (300 mL), sodium hydride (3.26 g, 55 wt %) and tetrabutylammonium iodide (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 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 extracted with dichloromethane. The extract was washed successively with water and saturated brine, dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated. Recrystallization of the residue from ethyl acetate/hexane gave the title compound (19.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883788B2
Source datasetuspto-grants-2014_11
ORD IDord-59950978c44444f7b957c7ddf24a5b57
Source noteuspto-grants-2014_11