HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → ethyl 5-bromo-2H-indazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-bromo-1H-indazole-3-carboxylic Acid | HCID 7157358 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 5-bromo-2H-indazole-3-carboxylate | HCID 12689364 | — |
Reaction Steps
3 g of 5-bromo-1H-indazole-3-carboxylic acid was dissolved in 60 mL of ethanol, added with 0.6 mL of concentrated sulfuric acid, and heated under reflux for 8 hours. After allowing to cool to room temperature, addition of water and extraction with ethyl acetate were conducted, and the resultant organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, dried over magnesium sulfate, and the solvent was evaporated, to afford 2.7 g of the title compound as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07429609B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-d77850c85fd540af9825519a7b12cb14 |
| Source note | uspto-grants-2008_09 |