Реакция #1929023

ord-8f3390d3066f4050b3ecf06ac985b53c

Уравнение реакции

O=C(Oc1cccc([N+](=O)[O-])c1)c1ccccc1
3-Nitrophenyl benzoate
O.O.[Cl][Sn][Cl]
tin (II) chloride dihydrate
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Nc1cccc(OC(=O)c2ccccc2)c1
3-aminophenyl benzoate
Выход 100.0%

Растворители

Условия реакции

Температура
100°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe reaction crude
  2. 2
    Температураto cool to room temperature
  3. 3
    ЭкстракцияThe crude material was extracted with dichloromethane (3×50 mL), magnesium sulfate
  4. 4
    workup.ADDITIONwas added to the organic phase
  5. 5
    Фильтрацияfiltered
  6. 6
    Другоеthe solvent was removed under reduced pressure

Методика

3-Nitrophenyl benzoate (2.7080 g, 11.144 mmol) and tin (II) chloride dihydrate (12.564 g, 55.720 mmol) were dissolved in 60 mL of ethanol and heated at 100° C. for 1 hour. The reaction crude was allowed to cool to room temperature, and an aqueous solution of sodium carbonate was added until pH 8. The crude material was extracted with dichloromethane (3×50 mL), magnesium sulfate was added to the organic phase, filtered and the solvent was removed under reduced pressure, thus affording 2.374 g (11.143 mmol, yield=100%) of 3-aminophenyl benzoate.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08945522B2uspto-grants-2015_02