Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178427873 | HCID 178427873 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 23075699 | HCID 23075699 | 75% |
Reaction Steps
Into 17.1 g (82.1 mmol) of 5-hydroxy-4-methyl-1-iso-propyl-3-trifluoromethyl-1H-pyrazole in 100 ml of 2-propanol was added 23.0 g (410.7 mmol) of powdery potassium hydroxide at room temperature, followed stirring. Furthermore, stirring was continued while an excess amount of chlorodifluoromethane was introduced into the reaction solution. Thereafter, the reaction temperature once rose to 70° C. by exothermic heat and then returned to room temperature after 2 hours. After the completion of the reaction was confirmed, the reaction solution was poured into water and extracted with ethyl acetate. The resulting organic layer was washed with water and saline, successively, and then dried over anhydrous magnesium sulfate. The solvent was removed by evaporation under reduced pressure and the residue was distilled to obtain 15.9 g (yield: 75.0%) of 5-difluoromethoxy-4-methyl-1-iso-propyl-3-trifluoromethyl-1H-pyrazole as a colorless transparent liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07256298B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-99709c42258045cc853496f9f42c9b65 |
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| Source note | uspto-grants-2007_08 |
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