HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 278159Erstellt: 25. Oktober 2026
Benzoyl Peroxide → 4-Cyano-3-fluorobenzyl bromide
https://huagongshe.com/reaction/278159
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzoyl Peroxide | HCID 7187 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 2-Fluoro-4-methylbenzonitrile | HCID 2778443 | — |
| Lösungsmittel | Carbon Tetrachloride | HCID 5943 | — |
| Produkt | 4-Cyano-3-fluorobenzyl bromide | HCID 2778466 | — |
Reaktionsschritte
To a solution of the product from Step C (22.2 g, 165 mmol) in 220 mL of carbontetrachloride was added N-bromosuccinimide (29.2 g, 164 mmol) and benzoylperoxide (1.1 g). The reaction was heated to reflux for 30 minutes, then cooled to room temperature. The solution was concentrated in vacuo to one-third the original volume, poured into EtOAc, washed with water, sat. aq. NaHCO3, and brine, then dried (Na2SO4), filtered, and concentrated in vacuo to provide the crude product. Analysis by 1H NMR indicated only partial conversion, so the crude material was resubjected to the same reaction conditions for 2.5 hours, using 18 g (102 mmol) of N-bromosuccinimide. After workup, the crude material was purified by silica gel chromatography (0-10% EtOAc/hexane) to provide the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06358985B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-0820a53ea7a745d798d5c82f7b972f94 |
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| Quellennotiz | uspto-grants-2002_03 |
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