Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 18780171 | HCID 18780171 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18780170 | HCID 18780170 | 89.8% |
Reaction Steps
Twenty mililiters (20 ml) of a mixture of sulfuric acid and water (v/v=1/1), and 7.3 g of 2-(4-chloro-3-isopropoxycarbonylphenyl)-6-ethoxycarbonyl-4-methyl-5-trifluoromethylpyridazin-3-one (the present compound 1-109) were mixed and heated for 7 hours on a 150° C. oil bath. The reaction solution was cooled to room temperature, poured into 100 ml of water. The precipitated crystals were filtered off, washed with 50 ml of water 3 times, dissolved with 200 ml of ethyl acetate and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to afford 4.88 g of 2-(4-chloro-5-carboxyphenyl)-4-methyl-5-trifluoromethylpyridazin-3-one (yield:89%).
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-cfec710acdc74a3ca7ce029de739b3f0 |
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| Source note | uspto-grants-2000_06 |
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