Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzoyl Peroxide | HCID 7187 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 2-Fluoro-4-methylpyridine | HCID 2737403 | — |
| Lösungsmittel | Carbon Tetrachloride | HCID 5943 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-Bromomethyl-2-fluoropyridine | HCID 13985168 | — |
Reaktionsschritte
To a solution of 2-fluoro-4-methylpyridine (0.510 g, 4.59 mmol) in 20 mL of carbon tetrachloride was added N-bromosuccinimide (0.899 g, 5.05 mmol) and benzoyl peroxide (0.148 g, 0.459 mmol). The mixture was heated to 90° C. for 1 h, and then additional benzoyl peroxide (0.074 g, 0.23 mmol) was added. After 20 h, the reaction was diluted with dichloromethane, washed 3× with water, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified via silica gel chromatography, eluting with 0-10% ethyl acetate in hexanes to provide the 4-(bromomethyl)-2-fluoropyridine that gave proton NMR spectra consistent with theory and a mass ion (ES+) of 191.9 (81Br) for [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08846702B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-26fd88478f0a49bca53fd2c9665016b2 |
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| Quellennotiz | uspto-grants-2014_09 |
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