HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904232Generated: October 30, 2026
Ethylene Glycol → 2-tert-Butyl-5-hydroxy-4-methylpyridazin-3(2H)-one
https://huagongshe.com/reaction/1904232
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
To 30 ml of ethylene glycol were added 20 g (0.01 mol) of 2-t-butyl-5-chloro-4-methyl-3(2H)-pyridazinone and 2.8 g (0.05 mol) of potassium hydroxide and the mixture was stirred at 130° C. for 4 hours. After allowing to cool, the mixture was poured into 200 ml of water and added with 20 ml of 6N hydrochloric acid. The precipitated crystals were gathered by filtration. After drying, the crystals were washed with 30 ml of hot isopropyl ether to obtain 1.7 g of 2-t-butyl-5-hydroxy-4-methyl-3(2H)-pyridazinone, m.p. 236.0°~239.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837217 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-291ca437f1d54b96ab8be57756f805ea |
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| Source note | uspto-grants-1989_06 |
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