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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-tert-butyl-5-chloro-4-methylpyridazin-3-(2H)-one | HCID 13822264 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-tert-Butyl-5-hydroxy-4-methylpyridazin-3(2H)-one | HCID 54713106 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04874861 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-ebecbf6eb66643808b8e15a3df470f59 |
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| Source note | uspto-grants-1989_10 |
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