Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | N-(4-Bromo-2-methylphenyl)acetamide | HCID 222277 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-bromo-1H-indazole | HCID 761929 | 38.8% |
Reaction Steps
tert-Butyl nitrite (8.34 g, 0.081 mol) was added dropwise, over 30 minutes, to a suspension of 4-bromo-2-methylacetanilide (12.3 g) in toluene (300 ml) at 65° C. and the mixture was stirred at 65° C. for 45 minutes and then at 90° C. for 3 hours. The mixture was cooled to room temperature and the solvent was removed in vacuo. The residue was purified by flash column chromatography on silica gel eluting with 2:1 diethyl ether:hexane to give 5-bromoindazole (4.12 g), as a sand-coloured solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07112553B1 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-2fda8f6d92014b63bcaf20807c91bf77 |
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| Source note | uspto-grants-2006_09 |
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