HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292797Generated: October 30, 2026
Water → 1-tert-butyl-5-methoxy-3-trifluoromethyl-1H-pyrazole
https://huagongshe.com/reaction/1292797
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178448751 | HCID 178448751 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-tert-butyl-5-methoxy-3-trifluoromethyl-1H-pyrazole | HCID 17862917 | 99.8% |
Reaction Steps
15.0 g (108.4 mmoles) of anhydrous potassium carbonate and 19.3 g (135.5 mmoles) of methyl iodide were added, at room temperature, to a solution of 18.8 g (90.3 mmoles) of 1-tert-butyl-3-trifluoromethyl-1H-pyrazol-5-ol dissolved in 100 ml of N,N-dimethylformamide. The mixture was stirred for 15 hours to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water, followed by extraction with diethyl ether. The resulting organic layer was washed with water and an aqueous sodium chloride solution in this order and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein, to obtain 20.0 g (yield: 99.8%) of 1-tert-butyl-5-methoxy-3-trifluoromethyl-1H-pyrazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238689B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-4c6cfb683dc84eb7891f056275e4fdc9 |
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| Source note | uspto-grants-2007_07 |
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