Реакция #1856346

ord-86e6e89343e044cc87262f865631c13c

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураunder reflux for 4 hours
  2. 2
    Фильтрацияfiltered
  3. 3
    ДругоеThe residue was recrystallized from ethanol

Методика

Eight grams (47.62 mmoles) of the above ester was treated with 6.3 ml (47.62 mmoles) of 3-chlorobenzyl bromide and 8 grams potassium carbonate in 70 ml acetonitrile under reflux for 4 hours. The mixture was diluted with 100 ml ethyl acetate, filtered, and stripped in vacuo. The residue was recrystallized from ethanol to give 9.5 g of 2-Carbomethoxy-4-(m-chlorophenylmethyloxy)-phenol (62% yield from 2,5-dihydroxybenzoic acid).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05380755uspto-grants-1995_01