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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352016Generated: October 28, 2026

Ethylene Glycol → 2-tert-Butyl-5-hydroxy-4-methylpyridazin-3(2H)-one

https://huagongshe.com/reaction/2352016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-oneHCID 13822264—
SolventWaterHCID 962—
Product2-tert-Butyl-5-hydroxy-4-methylpyridazin-3(2H)-oneHCID 54713106—

Reaction Conditions

Temperature130 °C

Reaction Steps

(Method A): A mixture of 2.0 g (0.01 mol) of 2-tert.-butyl-5-chloro-4-methyl-3(2H)-pyridazinone and 2.8 g (0.05 mol) of potassium hydroxide was added to 30 ml of ethylene glycol and stirred at 130° C. for 4 hours. After allowing to cool, the reaction liquid was poured into 200 ml of water and added with 20 ml of 6N hydrochloric acid. The crystals thus precipitated were collected by filtration. After drying, the crystals were washed with 30 ml of hot isopropyl ether to give 1.7 g of 2-tert.-butyl-5-hydroxy-4-methyl-3(2H)-pyridazinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874861
Source datasetuspto-grants-1989_10
ORD IDord-ebecbf6eb66643808b8e15a3df470f59
Source noteuspto-grants-1989_10