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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904234Generated: November 3, 2026

Water → 2-t-butyl-4-chloro-5-[4-(2-ethoxyethoxy)benzyloxy]-3(2H)-pyridazinone

https://huagongshe.com/reaction/1904234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Ethoxyethoxy)-benzyl bromideHCID 14671793—
Reactant2-tert-Butyl-4-chloro-5-hydroxypyridazin-3(2H)-oneHCID 54686946—
SolventDimethylformamideHCID 6228—
Product2-t-butyl-4-chloro-5-[4-(2-ethoxyethoxy)benzyloxy]-3(2H)-pyridazinoneHCID 1467179458.5%

Reaction Steps

In 10 ml of N,N-dimethylformamide were dissolved 1.0 g of 2-t-butyl-4-chloro-5-hydroxy-3(2H)-pyridazinone and 1.3 g of 4-(2-ethoxyethoxy)-benzyl bromide, and then 1.0 g of anhydrous potassium carbonate was added thereto. The mixture was heated with stirring on an oil bath at 90° to 100° C. for 3 hours, poured into water, extracted with benzene, washed with water and dried over anhydrous sodium sulfate. Benzene was distilled off under reduced pressure and the resulting oil was purified by means of column chromatography (on silica gel, eluting with benzene/ethyl acetate=18/1) and recrystallization (from n-hexane-benzene) to obtain 1.1 g of the aimed compound, m.p. 82.0°~83.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837217
Source datasetuspto-grants-1989_06
ORD IDord-4aa05d62b5d942c1a6e66b3c792940ce
Source noteuspto-grants-1989_06