HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromophenylhydrazine hydrochloride → Ethyl 1-(3-bromophenyl)-5-methyl-1h-pyrazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromophenylhydrazine hydrochloride | HCID 33757 | — |
| Reactant | Ethyl 2,4-dioxovalerate | HCID 69208 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 1-(3-bromophenyl)-5-methyl-1h-pyrazole-3-carboxylate | HCID 18549277 | 85% |
Reaction Steps
A solution of 3-bromophenylhydrazine hydrochloride (2 g, 8.9 mmol) and ethyl-2,4-dioxovalerate (1.69 g, 10.7 mmol) in acetic acid (44 ml) was refluxed for 16 hours. The reaction was cooled to room temperature and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water. The organic layer was washed with water, saturated bicarbonate and brine, and then dried over sodium sulfate, filtered and concentrated in vacuo. The crude product, thus obtained, was purified by silica-gel column chromatography (4.8:0.2 hexanes/ethyl acetate) to give the product (2.34 g, 84%) as a syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07589116B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-4bd1734b898549f9ae0564afeda9c50e |
| Source note | uspto-grants-2009_09 |