HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 6-bromo-1H-indazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 6-Bromo-1H-indazole-3-carboxylic acid | HCID 24728028 | — |
| Product | Ethyl 6-bromo-1H-indazole-3-carboxylate | HCID 51358649 | — |
Reaction Steps
To a stirred solution of 6-bromo-1H-indazole-3-carboxylic acid (5 g, 21 mmol) in ethanol (160 Ml), thionyl chloride (8 Ml, 104 mmol; SOCl2) was added. The mixture was refluxed for 3 h, cooled to room temperature, and concentrated under reduced pressure. Ethyl acetate was added. The organic layer was washed with saturated sodium bicarbonate solution, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, DCM:MeOH=9:1) to give ethyl 6-bromo-1H-indazole-3-carboxylate (2.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754209B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-8822949004f946debace9372bfdae753 |
| Source note | uspto-grants-2014_06 |