Reacción #1261632

ord-ad74d5cace7347d685d0435d7d99b4fa

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawhile heating
  2. 2
    Temperaturarefluxing
  3. 3
    OtroThe deposit was removed by filtration
  4. 4
    Concentraciónthe filtrate was concentrated

Procedimiento

A mixture of 52.35 g (368.1 mmol) of 1-methylnaphthalene, 68.79 g (368.5 mmol) of N-bromosuccinimide (NBS), 0.45 g (1.86 mmol) of benzoyl peroxide (BPO) and 250 ml of carbon tetrachloride was stirred for 6 hours while heating and refluxing. The deposit was removed by filtration, and the filtrate was concentrated to obtain 84.64 g (purity: 90.4%, yield: 94%) of an oily crude product of 1-(bromomethyl)naphthalene.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07838130B2uspto-grants-2010_11