Реакция #997890

ord-c24bc5bd7b6447eb803f60e50d8e00ba

Уравнение реакции

OCc1c2ccccc2cc2ccccc12
anthracen-9-yl-methanol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
BrBr
Bromine
BrCc1c2ccccc2cc2ccccc12
9-bromomethyl-anthracene
Выход 69.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.WAITrefrigerated at 5° C. overnight
  2. 2
    ТемператураThe solution was cooled to 0° C. for 30 minutes
  3. 3
    Фильтрацияfiltered
  4. 4
    ПромывкаThe residue was washed with cold acetonitrile
  5. 5
    Другоеpurified by recrystallization from chloroform

Методика

A solution of triphenylphosphine (16.44 g, 100.8 mmol) in acetonitrile (120 mL) was flushed with nitrogen for 20 minutes. Bromine (3.3 mL) was added and a solution of anthracen-9-yl-methanol (15.0 g, 72.0 mmol) in acetonitrile (100 mL) was added dropwise. The mixture was stirred for 2 hours at room temperature and refrigerated at 5° C. overnight. The solution was cooled to 0° C. for 30 minutes and filtered. The residue was washed with cold acetonitrile and purified by recrystallization from chloroform to give 9-bromomethyl-anthracene as yellow crystals (13.47 g, 69% yield). 1H NMR (CDCl3) δ 8.51 (1H, s), 8.32 (2H, d), 8.05 (2H, d), 7.66 (2H, dd), 7.52 (2H, dd), 5.56 (2H, s).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08022214B2uspto-grants-2011_09