HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1883630Erstellt: 26. Oktober 2026
Azobisisobutyronitrile → 3-(Bromomethyl)-4-chloro-1,1'-biphenyl
https://huagongshe.com/reaction/1883630
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Azobisisobutyronitrile | HCID 6547 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 4-Chloro-3-methyl-1,1'-biphenyl | HCID 20329672 | — |
| Lösungsmittel | Carbon Tetrachloride | HCID 5943 | — |
| Produkt | 3-(Bromomethyl)-4-chloro-1,1'-biphenyl | HCID 23508194 | 86,8% |
Reaktionsschritte
3.90 g (19.2 mmol) of 4-chloro-3-methylbiphenyl was dissolved in 100 ml of carbon tetrachloride and to this solution was added 632 mg (3.85 mmol) of 2,2′-azobisisobutylonitrile, and the mixture was stirred at room temperature for 15 minutes. To this solution was added 3.43 g (19.2 mmol) of N-bromosuccinimide, and the mixture was stirred for 3.5 hours while heating under reflux. To the reaction solution was further added 632 mg (3.85 mmol) of 2,2′-azobisisobutyronitrile and 300 mg (1.69 mmol) of N-bromosuccinimide, and the mixture was stirred for 2 hours under reflux with heating. The reaction mixture was filtrated, and the filtrate was concentrated. The residue was subjected to silica gel column chromatography (eluant: hexane) to obtain 4.69 g of 2-chloro-5-phenylbenzyl bromide in the form of colorless transparent oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06762197B2 |
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| Quelldatensatz | uspto-grants-2004_07 |
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| ORD ID | ord-c2045f944fe748f0a0f78d25d3bdf080 |
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| Quellennotiz | uspto-grants-2004_07 |
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