HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 5-(Bromomethyl)-1H-indazole--hydrogen bromide (1/1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 1-Acetyl-5-(acetoxymethyl)indazole | HCID 10799569 | — |
| Product | 5-(Bromomethyl)-1H-indazole--hydrogen bromide (1/1) | HCID 22661441 | — |
Reaction Steps
A suspension of 1-acetyl-5-(acetoxymethyl)indazole (12-3) (3.0 g, 13 mmol) in aqueous hydrobromic acid (15 mL, 226 mmol) was stirred at room temperature for 25 hours. The solid was collected on a Buchner funnel and dried under vacuum for 12 hours. The filtrate was stirred at room temperature for additional 24 hours and more solid was collected. After drying under vacuum, title compound was obtained as a yellow solid (12-4, 3.48 g, 92%) which was used in the next synthesis step without further purification. 1H NMR (CDCl3) δ4.88 (s, 2H), 7.43 (d, 1H, J=8.8), 7.56 (d, 1H, J=8.8 Hz), 7.87 (s, 1H), 8.10 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506761B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-093db36fc3424b989c7b53b45a063393 |
| Source note | uspto-grants-2003_01 |