Реакция #58712

ord-9c2b8a9d4e16458db3b64caa59ba5bac

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe mixture was cooled
  2. 2
    Фильтрацияthe precipitated product was recovered by filtration
  3. 3
    Другоеdried under vacuum at 65° C

Методика

151.8 g (0.49 mol) of 1-(4-benzyloxy-3-nitrophenyl)-2-chloroethanol was dissolved in THF (0.75 L) and treated dropwise with NaOH (4 mol/L, 182 mL, 0.73 mol). After 1 hour, AcOH (30 mL) was added followed by water (2.5 L). The mixture was cooled and the precipitated product was recovered by filtration and dried under vacuum at 65° C. Yield: 133.0 g (99.3%); mass spectroscopy: [M+H]+=272; m.p.=66° C.; e.e. 99.5%.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07423146B2uspto-grants-2008_09