HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628508Generated: October 29, 2026
Dimethylformamide → 5-(4-methoxy-3-methyl-phenyl)-1-methyl-1H-pyrazole
https://huagongshe.com/reaction/628508
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178488675 | HCID 178488675 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(4-methoxy-3-methyl-phenyl)-1-methyl-1H-pyrazole | HCID 116869101 | — |
| Product | 3-(4-methoxy-3-methyl-phenyl)-1-methyl-1H-pyrazole | HCID 118236253 | — |
Reaction Steps
At room temperature, to a mixture of 3-(4-methoxy-3-methyl-phenyl)-1H-pyrazole (described in Reference Preparation example 44) 5.38 g and N,N-dimethylformamide 100 ml was added 55% sodium hydride 1.5 g and the resulting mixture was stirred for a half hour and thereto was added methyl iodide 7.9 g. The resulting mixture was stirred for twelve hours and thereto was added water, and then the resulting mixture was extracted with ethyl acetate. The organic layer was washed with water, and was dried over anhydrous magnesium sulfate and was then concentrated under reduced pressure. The resulting residue was subjected to a silica gel column chromatography to give 3-(4-methoxy-3-methyl-phenyl)-1-methyl-1H-pyrazole 2.9 g and 5-(4-methoxy-3-methyl-phenyl)-1-methyl-1H-pyrazole 1.0 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09314023B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-f6d42db8ea6445028d413876ea8015e4 |
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| Source note | uspto-grants-2016_04 |
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