反应 #41354

ord-fe19162b385a4d96923b629a75311512

反应方程式

CC(C)N1CCN2CCN(C(C)C)P1N(C(C)C)CC2
2,8,9-triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane
O=CCOc1ccccc1
2-Phenoxyacetaldehyde
O=S(=O)([O-])[O-].[Mg+2]
magnesium sulfate
CC[N+](=O)[O-]
nitroethane
CC(C(O)COc1ccccc1)[N+](=O)[O-]
subtitle compound
收率 81.0%
CC(C(O)COc1ccccc1)[N+](=O)[O-]
3-Nitro-1-phenoxy-butan-2-ol
收率 81.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤filtered through celite and
  2. 2
    浓缩concentrated
  3. 3
    其他Purification by column chromatography (SiO2, dichloromethane/t-butyl methyl ether)

实验过程

2-Phenoxyacetaldehyde (1.36 g, 10 mmol) was added to a suspension of anhydrous magnesium sulfate (2.65 g, 22 mmol) in nitroethane (7.0 mL) under an argon atmosphere. After 5 min a solution of 2,8,9-triisopropyl-2,5,8,9-tetraaza-1-phosphabicyclo[3,3,3]undecane (0.30 g, 1.0 mmol) in nitromethane (3.0 mL) was added. The mixture was vigorously stirred for 5 days at r.t., filtered through celite and concentrated. Purification by column chromatography (SiO2, dichloromethane/t-butyl methyl ether) gave the subtitle compound as an oil (1.7 g, 81%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07728030B2uspto-grants-2010_06