تفاعل #80262

ord-2a97706acabd438eb775c9adf442792f

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooled in an ice bath
  2. 2
    workup.STIRRINGThe reaction was stirred for 45 minutes
  3. 3
    workup.ADDITIONafter the addition
  4. 4
    ترشيحThe resulting solid was collected by filtration
  5. 5
    أخرىdried in vacuo

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05616505uspto-grants-1997_04