HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421622Generated: November 1, 2026
Sulfuric Acid → 2-(4-Chloro-2-fluoro-5-hydroxyphenyl)-4-methyl-5-(trifluoromethyl)-3(2H)-pyridazinone
https://huagongshe.com/reaction/1421622
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 18780174 | HCID 18780174 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Chloro-2-fluoro-5-hydroxyphenyl)-4-methyl-5-(trifluoromethyl)-3(2H)-pyridazinone | HCID 9949091 | 50% |
Reaction Steps
Three mililiters (3 ml) of a mixture of sulfuric acid and water (v/v=2/1), and 1.5 g of 2-(4-chloro-2-fluoro-5-isopropoxyphenyl)-6-ethoxycarbonyl-4-methyl-5-trifluoromethylpyridazin-3-one (the present compound 1-31) were mixed and heated for 6 hours on a 130° C. oil bath. The reaction solution was cooled to room temperature, poured into 50 ml of water. The precipitated crystals were filtered off and washed with 50 ml of water twice. The crystals were dissolved with 100 ml of ethyl acetate and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the obtained crystals were washed with 20 ml of n-hexane to afford 0.55 g of 2-(4-chloro-2-fluoro-5-hydroxyphenyl)-4methyl-5-trifluoromethylpyridazin-3-one (yield:50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06077953 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-489a1b74713d48e28e5d28c5f5b8cb2b |
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| Source note | uspto-grants-2000_06 |
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