HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → Tert-butyl 3-(bromomethyl)-6-fluoro-1H-indazole-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | tert-butyl 6-fluoro-3-methyl-1H-indazole-1-carboxylate | HCID 53779261 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Tert-butyl 3-(bromomethyl)-6-fluoro-1H-indazole-1-carboxylate | HCID 10568325 | 60.9% |
Reaction Steps
12.68 g (50.7 mmol) 6-Fluoro-3-methyl-indazole-1-carboxylic acid tert-butyl ester, prepared as in Part C, is combined with 9.92 g (55.7 mmol, 1.1 equiv) N-Bromosuccinimide and 1.23 g (5.1 mmol, 0.1 equiv) Benzoyl peroxide in 600 mL CCl4 and refluxed 10 h. The reaction mixture is filtered and the filtrate concentrated in vacuo and purified by flash chromatography on 300 g silica gel eluted successively with DCM/Hexanes (1:2, 3 L), (1:1, 3 L). Appropriate fractions were combined and concentrated in vacuo to give 10.18 g (30.9 mmol) of 3-Bromomethyl-6-fluoro-1-tert-butoxycarbonyl-1H-indazole as an amber oil: 1H NMR (CDCl3, 300 MHz) δ7.82 (m, 2H), 7.13 (m, 1H), 4.76 (s, 2H), 1.72 (s, 9H); TLC Rf =0.17 (EtOAc/Hexanes, 1:19).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859007 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-8ceaa4b03f984f8a8e165baaf3bc9ecc |
| Source note | uspto-grants-1999_01 |