Réaction #2439926

ord-16a2cde627f94a1c95e63b11caaead5e

Équation de réaction

Cc1ccnc(-c2ccc(F)cc2)c1
2-(p-fluorophenyl)-4-methyl-pyridine
O=C1CCC(=O)N1Br
N-bromosuccinimide
O=C(OOC(=O)c1ccccc1)c1ccccc1
benzoylperoxide
Fc1ccc(-c2cc(CBr)ccn2)cc1
2-(p-fluorophenyl)-4-bromomethyl-pyridine
Rendement 88.7%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureat reflux temperature
  2. 2
    Autreirradiated by means of an ordinary 250-W UV lamp for 4 hrs
  3. 3
    TempératureAfterwards, the reaction mixture was cooled
  4. 4
    Autresubsequently triturated with Et2O/petroleum benzine
  5. 5
    AutreThe precipitate was removed by filtration
  6. 6
    Concentrationthe filtrate was concentrated in vacuo

Mode opératoire

A mixture of 2-(p-fluorophenyl)-4-methyl-pyridine (0.5 g, 2.67 mmol), N-bromosuccinimide (0.48 g, 2.69 mmol), and a catalytic amount of benzoylperoxide in CCl4 (50 ml) was stirred at reflux temperature and irradiated by means of an ordinary 250-W UV lamp for 4 hrs. Afterwards, the reaction mixture was cooled and subsequently triturated with Et2O/petroleum benzine. The precipitate was removed by filtration, and the filtrate was concentrated in vacuo to give 2-(p-fluorophenyl)-4-bromomethyl-pyridine (0.63 g, 88%, unstable) as a dark yellow oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE041425E1uspto-grants-2010_07