HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027180Generated: October 30, 2026
Salicylaldehyde oxime → HCID 86710575, compound
https://huagongshe.com/reaction/1027180
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylaldehyde oxime | HCID 7200 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Bromo-4-iodo-2-methoxybenzene | HCID 12187202 | — |
| Reactant | HCID 178526745 | HCID 178526745 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86710575 | HCID 86710575 | 60.5% |
Reaction Steps
A mixture of 1-bromo-4-iodo-2-methoxybenzene (3.99 g, 12.75 mmol), 3-nitro-1H-pyrazole (1.730 g, 15.30 mmol), Salicylaldoxime (0.350 g, 2.55 mmol), Cu2O (0.146 g, 1.020 mmol) and Cs2CO3 (6.23 g, 19.13 mmol) in DMF (13 mL) was degassed with N2 and heated at 95° C. overnight. After cooling to RT, the mixture was filtered through celite and rinsed with EtOAc. The filtrate was washed with water and brine. The organic solution was dried over Na2SO4, filtered and concentrated in vacuo. The residue was suspended in 5% MeOH/DCM, and the precipitate filtered, rinsed with 5% MeOH/DCM, and dried to give 2.3 g of 1-(4-bromo-3-methoxyphenyl)-3-nitro-1H-pyrazole as a white solid. The filtrate from the above work up was purified by silica gel chromatography (EtOAc/Heptane=10:90 to 50:50) to give an additional 760 mg of 1-(4-bromo-3-methoxyphenyl)-3-nitro-1H-pyrazole as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08729263B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-4806e4de634243e1bc28cb14f19ae4d2 |
|---|
| Source note | uspto-grants-2014_05 |
|---|