HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027171Generated: October 30, 2026
Salicylaldehyde oxime → (1-(4-bromo-3-methoxyphenyl)-1H-pyrazol-4-yl)methanol
https://huagongshe.com/reaction/1027171
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylaldehyde oxime | HCID 7200 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Hydroxymethylpyrazole | HCID 3015210 | — |
| Reactant | 2-Bromo-3-iodoanisole | HCID 23636210 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (1-(4-bromo-3-methoxyphenyl)-1H-pyrazol-4-yl)methanol | HCID 86710564 | 55.4% |
Reaction Steps
A mixture of 4-(hydroxymethyl)pyrazole (500 mg, 5.10 mmol), salicylaldoxime (140 mg, 1.019 mmol), cesium carbonate (4.98 g, 15.29 mmol), cuprous oxide (58.2 mg, 0.306 mmol), iodobromoanisole (1.59 g, 5.10 mmol) and N,N-dimethyl-formamide (10 mL) were combined in a microwave vial fitted with an N2 inlet and magnetic stir bar. The reaction mixture was stirred under a nitrogen atmosphere at 90° C. overnight. The reaction mixture was cooled to RT, then filtered through celite, and the filtrate was concentrated in vacuo. The crude material was purified by column chromotography (10% to 60% EtOAc in heptanes) to give (1-(4-bromo-3-methoxyphenyl)-1H-pyrazol-4-yl)methanol (800 mg, MS: 285.3 [M+H+].)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729263B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-2e83621e5fee4a4e85f60d0c7bd8d5e1 |
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| Source note | uspto-grants-2014_05 |
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