Reaktion #2073

ord-66715e3038e443c89124069570855fa8

Reaktionsgleichung

CCCCCC(N)CC(P(=O)(OCC)OCC)P(=O)(OCC)OCC
tetraethyl 3-aminooctane-1,1-bisphosphonate
C[Si](C)(C)Br
bromotrimethylsilane
CCCCCC(N)CC(P(=O)([O-])[O-])P(=O)([O-])O.[NH4+].[NH4+].[NH4+]
3-aminooctane-1,1-bisphosphonic acid, triammonium salt

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthe mixture was concentrated under vacuum
  2. 2
    workup.ADDITIONTo the residue was added 3N NH4OH (8 mL) which
  3. 3
    SonstigeThe solvent was removed in vacuo
  4. 4
    Einengenthe residue concentrated from methanol (2 mL)

Vorschrift

To a solution of tetraethyl 3-aminooctane-1,1-bisphosphonate (0.45 g, 1.12 mmol) in dry dichloromethane (1.1 mL) was added bromotrimethylsilane (1.05 mL, 7.85 mmol) via syringe. After 18 hours, the mixture was concentrated under vacuum. To the residue was added 3N NH4OH (8 mL) which was stirred for 30 minutes at room temperature. The solvent was removed in vacuo and the residue concentrated from methanol (2 mL) to give 0.40 g of 3-aminooctane-1,1-bisphosphonic acid, triammonium salt as a white powder.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728650uspto-grants-1998_03