反应 #684962

ord-7f09f82c6daf47efaf0b14092852a6a1

反应方程式

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
收率 72.6%
COc1cccc(C(O)CN)c1
2-Amino-1-(3-methoxyphenyl)-1-ethanol
收率 72.6%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The catalyst was removed by filtration
  2. 2
    workup.ADDITIONthe filtrate was diluted with ether
  3. 3
    其他precipitates
  4. 4
    其他were removed by filtration
  5. 5
    浓缩the obtained filtrate was concentrated

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07897387B2uspto-grants-2011_03