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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352023Generated: November 1, 2026

Water → 2-t-butyl-5-(p-fluorobenzyloxy)-4-methyl-3(2H)-pyridazinone

https://huagongshe.com/reaction/2352023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-Fluorobenzylic alcoholHCID 68022—
Reactant2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-oneHCID 13822264—
SolventDimethylformamideHCID 6228—
Product2-t-butyl-5-(p-fluorobenzyloxy)-4-methyl-3(2H)-pyridazinoneHCID 1382513762.2%

Reaction Steps

To a solution of 0.63 g (0.005 mol) of p-fluorobenzyl alcohol dissolved in 20 ml of N,N-dimethylformamide was added 0.24 g of 55% sodium hydride at room temperature under stirring. After addition, the resulting mixture was further stirred at room temperature for fifteen minutes. The reaction liquid was added dropwise with 1.0 g of 2-t-butyl-5-chloro-4-methyl-3(2H)-pyridazinone, and was stirred at room temperature for eight hours. The reaction mixture was poured into 200 ml of water and then extracted with 50 ml of benzene. The resulting benzene layer was washed successively with 50 ml of 10% sodium hydroxide, 50 ml of 1N-hydrochloric acid, and 100 ml of water, dried over anhydrous sodium sulfate, and freed of solvent by distillation to give 1.5 g of crude product. The crude product was recrystallized from 20 ml of hexane to obtain 0.9 g of 2-t-butyl-5-(p-fluorobenzyloxy)-4-methyl-3(2H)-pyridazinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874861
Source datasetuspto-grants-1989_10
ORD IDord-b8c5a5d0778049ce95bddad55a7a06ec
Source noteuspto-grants-1989_10