Реакция #51652

ord-6135df3391b94ab680a5652fa0de43f5

Уравнение реакции

CC(=O)Nc1ccc(O)cc1
4-acetamidophenol
COC(=O)c1ccc(B(O)O)cc1
(4-methoxycarbonylphenyl)boronic acid
COC(=O)c1ccc(Oc2ccc(NC(C)=O)cc2)cc1
methyl 4-(4-acetamidophenoxy)benzoate
Выход 75.1%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеDry air
  2. 2
    Другоеfor 16 hours
  3. 3
    Другоеat room temperature
  4. 4
    КонцентрированиеThe resulting material is concentrated
  5. 5
    Другоеpurified by flash column chromatography (25-50% EtOAc in heptane)

Методика

Dry air is bubbled through a solution of 4-acetamidophenol (320 mg, 2.1 mmol), copper(II) acetate (384 mg, 2.1 mmol), TEA (1.5 mL, 10.5 mol), (4-methoxycarbonylphenyl)boronic acid (760 mg, 4.2 mmol), and powdered molecular sieves (2 g) in CH2Cl2 (21 mL) for 16 hours at room temperature. The resulting material is concentrated and purified by flash column chromatography (25-50% EtOAc in heptane) to give methyl 4-(4-acetamidophenoxy)benzoate (450 mg, 75%). 1H NMR (300 MHz, DMSO) δ 8.01, 7.54, 7.27, 7.05, 6.98, 3.92, 2.22.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06852716B2uspto-grants-2005_02