Реакция #684962

ord-7f09f82c6daf47efaf0b14092852a6a1

Уравнение реакции

O=C[O-].[NH4+]
ammonium formate
COc1cccc(C(O)C[N+](=O)[O-])c1
compound
COc1cccc(C(O)C[N+](=O)[O-])c1
1-(3-Methoxyphenyl)-2-nitro-1-ethanol
COc1cccc(C(O)CN)c1
title compound
Выход 72.6%
COc1cccc(C(O)CN)c1
2-Amino-1-(3-methoxyphenyl)-1-ethanol
Выход 72.6%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe catalyst was removed by filtration
  2. 2
    workup.ADDITIONthe filtrate was diluted with ether
  3. 3
    Другоеprecipitates
  4. 4
    Другоеwere removed by filtration
  5. 5
    Концентрированиеthe obtained filtrate was concentrated

Методика

Palladium-carbon (10%, 0.64 g) and ammonium formate (4.8 g) were added to a mixed solution of the compound of Example B142 (3.0 g, 15 mmol) in tetrahydrofuran (43 ml) and methanol (43 ml), and this mixture was stirred at room temperature for 18 hours. The catalyst was removed by filtration, the filtrate was diluted with ether, precipitates were removed by filtration, and the obtained filtrate was concentrated to give the title compound (1.82 g). This compound was used in the following reaction without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07897387B2uspto-grants-2011_03