Реакция #78906

ord-f4b44a2492fb47cf93b9bdf88797f5df

Уравнение реакции

CCOC(=O)c1ccc(Br)cc1
4-bromo-benzoic acid ethyl ester
CCOP([O-])OCC
diethyl phosphite
CCOC(=O)c1ccc(P(=O)(OCC)OCC)cc1
oil
Выход 67.9%
CCOC(=O)c1ccc(P(=O)(OCC)OCC)cc1
4-(Diethoxyphosphoryl)-benzoic Acid Ethyl Ester
Выход 67.9%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеA sealed pressure flask, flushed with N2
  2. 2
    workup.ADDITIONcontaining
  3. 3
    Температураheated at 90° C. for 18 hours
  4. 4
    ФильтрацияThe reaction mixture was filtered through celite
  5. 5
    Промывкаthe celite was washed with EtOAc (3×30 mL) until the filtrate
  6. 6
    СушкаThe combined organics were dried over Na2SO4
  7. 7
    Концентрированиеconcentrated on a rotary evaporator
  8. 8
    ДругоеThe desired product was purified by silica gel flash chromatography

Методика

A sealed pressure flask, flushed with N2, containing a mixture of 4-bromo-benzoic acid ethyl ester (2a) (5 g, 0.0218 mol), diethyl phosphite (3.093 mL, 0.024 mol), NMM (2.88 mL, 0.0262 mmol) and Pd(PPh3)4 (2.017 g, 0.00175 mol) in acetonitrile (20 mL) was stirred at ambient temperature for 5-10 min, then heated at 90° C. for 18 hours. The reaction mixture was filtered through celite, and the celite was washed with EtOAc (3×30 mL) until the filtrate showed little or no evidence of product by HPLC. The combined organics were dried over Na2SO4 and concentrated on a rotary evaporator. The desired product was purified by silica gel flash chromatography to give a pale yellow oil (4.24 g). 1H NMR (300 MHz, CDCl3) δ (ppm)) 1.36 (m, 6H), 1.42 (t, J=7 Hz, 3H), 4.16 (m, 4H), 4.42 (q, J=7 Hz, 2H), 7.93 (m, 2H), 8.15 (m, 2H). 31P NMR (121 MHz, CDCl3) δ17.63.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06713462B2uspto-grants-2004_03