Реакция #10703

ord-966493f923fe4472bb4fc0c0429b9e71

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ПромывкаIn this case, the product was eluted with ether:hexanes (1:10)

Методика

This phenol was prepared, as described above, from a theoretical yield of 3.9 mmol of diazotized 2,6-diisopropylaniline and a phenolate solution comprised of 2-(9-Anthracenyl)-4-methylphenol (0.63 g), water (20 mL), NaOH (20 mmol), pyridine (2 mL), and benzene (4 mL). In this case, the product was eluted with ether:hexanes (1:10). Yield=0.30 g (29%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07094848B2uspto-grants-2006_08