Réaction #57524

Équation de réaction

(6-bromo-3-methyl-benzofuran-2-yl)-(2,4-dichloro-phenyl)-methanone

N-bromosuccinimide

2,2′-azobisisobutyronitrile

→

desired product

Rendement 78.9%

(6-bromo-3-bromomethyl-benzofuran-2-yl)-(2,4-dichloro-phenyl)-methanone

Rendement 78.9%

Solvants

carbon tetrachloride

Conditions de réaction

Traitement

1. 1
   TempératureThe reaction mixture was refluxed for 6 h
2. 2
   Filtrationfiltered
3. 3
   ConcentrationThe filtrate was concentrated
4. 4
   Autrethe crude product was triturated with 10% EtOAc/hexane

Mode opératoire

To a solution of (6-bromo-3-methyl-benzofuran-2-yl)-(2,4-dichloro-phenyl)-methanone (3.0 g, 7.81 mmol) in carbon tetrachloride (30 mL) was added N-bromosuccinimide (1.46 g, 8.2 mmol) and 2,2′-azobisisobutyronitrile (128 mg, 0.78 mmol). The reaction mixture was refluxed for 6 h, then filtered. The filtrate was concentrated and the crude product was triturated with 10% EtOAc/hexane to afford the desired product as a pale yellow solid (2.85 g, 78.9%). This material was used in the subsequent step without further purification.

Source