Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | HCID 178510261 | HCID 178510261 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 66718904 | HCID 66718904 | 65.5% |
Reaction Steps
18.5 g (0.10 mole) of the 3-cyano-5-hydroxy-1-phenylpyrazole synthesized in Reference Example 4 was dissolved in 35.0 g (0.15 mole) of a 24% aqueous potassium hydroxide solution. To the solution being stirred at room temperature was dropwise added 9.7 g (0.12 mole) of a 37% formalin solution, followed by stirring at the same temperature for 1 hour. Then, there were added 70.0 g (0.3 mole) of a 24% aqueous potassium hydroxide solution and 100 ml of acetonitrile. Therein was blown 17.3 g (0.20 mole) of chlorodifluoromethane at room temperature in 2 hours, followed by stirring at room temperature for 2 hours to give rise to a reaction. After the reaction, the organic layer which appeared by phase separation, was concentrated under reduced pressure to obtain 24.6 g (purity: 70.6%, yield: 65.5%) of a crude solution of title compound. The crude solution was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1) to obtain a title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812175B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-1a3c36433c0141bdb618bf7f3fde378b |
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| Source note | uspto-grants-2010_10 |
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