HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44199Generated: October 29, 2026
Hydrochloric Acid → 4-(2-Ethylphenyl)-5-hydroxy-2-methyl-3(2H)-pyridazinone
https://huagongshe.com/reaction/44199
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-(2-ethylphenyl)-5-methoxy-2-methyl-3(2H)-pyridazinone | HCID 57437317 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(2-Ethylphenyl)-5-hydroxy-2-methyl-3(2H)-pyridazinone | HCID 57437316 | 68.1% |
Reaction Steps
After 50 mL of water, 4.657 g of potassium hydroxide (content, 85%) and 5 mL of 1,4-dioxane were added to 3.193 g of 4-(2-ethylphenyl)-5-methoxy-2-methyl-3(2H)-pyridazinone (Compound II-1), the mixture was stirred and heated under reflux for 36 hours. After cooling, concentrated hydrochloric acid was added to the reaction mixture to acidify, to which 10 ml of water and 100 ml of ethyl acetate were added. The resulting mixture was filtered to remove insoluble substances and the filtrate was separate to two phase. The organic layer was washed with water and then a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off. The solid obtained was washed with a mixed solvent of ethyl acetate and hexane (1:2) to yield 2.050 g of the title compound as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541414B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-c3c4d5f370854d2992a841ac5930e52b |
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| Source note | uspto-grants-2013_09 |
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