反应 #80262

ord-2a97706acabd438eb775c9adf442792f

反应方程式

COC(=O)CC12CC3CC(C1)CC(c1ccccc1)(C3)C2
Methyl 3-phenyl-1-adamantaneacetate
F[B-](F)(F)F.O=[N+]=O
Nitronium tetrafluoroborate
COC(=O)CC12CC3CC(C1)CC(c1ccc([N+](=O)[O-])cc1)(C3)C2
methyl 3-(4-nitrophenyl)-1-adamantaneacetate

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度cooled in an ice bath
  2. 2
    workup.STIRRINGThe reaction was stirred for 45 minutes
  3. 3
    workup.ADDITIONafter the addition
  4. 4
    过滤The resulting solid was collected by filtration
  5. 5
    其他dried in vacuo

实验过程

Methyl 3-phenyl-1-adamantaneacetate, example 1, (78.8 g) was dissolved in acetonitrile (800 mL) and cooled in an ice bath while stirring under a nitrogen atmosphere. Nitronium tetrafluoroborate (40.8 g) in acetonitrile (800 mL) was added dropwise over 45 minutes. The reaction was stirred for 45 minutes after the addition, then poured into ice (985 g). The resulting solid was collected by filtration and dried in vacuo to give methyl 3-(4-nitrophenyl)-1-adamantaneacetate (55.9 g). Mass spectrum: (M+NH4)+ @347. Extraction of the aqueous phase with t-butyl methyl ether (2×800 mL) yeilded additional material including the lesser products, methyl 3-(2-nitrophenyl)-1-adamantaneacetate; Mass spectrum: (M+NH4)+ @347 and methyl 3-(2,4-dinitrophenyl)-1-adamantaneacetate; Mass spectrum: (M+NH4)+ @392.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05616505uspto-grants-1997_04