反応 #1483083

ord-f41422ae8c9e4910bda7808b0388f11a

反応方程式

NCC(CN)(CN)CN.[Cl-].[Cl-].[Cl-].[Cl-]
tetrakis(aminomethyl)methane tetrachloride
CO.C[O-].[Na+]
NaOMe MeOH
NCC(CN)(CN)CN
tetrakis(aminomethyl)methane

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他Tetrakis(aminomethyl)methane is prepared by a known procedure (Adil, K. et al., Solid State Sciences, 6 (2004), 1229-1235)
  2. 2
    その他A 50 mL flask is equipped with a reflux condenser and a magnetic stirrer
  3. 3
    温度refluxed for 4 hours
  4. 4
    温度cooled
  5. 5
    その他Methanol solution is decanted from the inorganic salts
  6. 6
    濃縮the combined organics are concentrated in vacuo
  7. 7
    workup.DISSOLUTIONThe residue is dissolved in methylene chloride (15 mL)
  8. 8
    ろ過filtered
  9. 9
    ろ過(0.45 micron filter) from the remaining inorganic salts

実験手順

Tetrakis(aminomethyl)methane is prepared by a known procedure (Adil, K. et al., Solid State Sciences, 6 (2004), 1229-1235). A 50 mL flask is equipped with a reflux condenser and a magnetic stirrer. The flask is charged with tetrakis(aminomethyl)methane tetrachloride (800 mg, 2.88 mmol), methanol (10 mL) and NaOMe/MeOH solution (2.10 g of 5.457M, 11.50 mmol). The mixture is stirred and refluxed for 4 hours, then cooled. Methanol solution is decanted from the inorganic salts, and the salts are re-suspended in absolute ethanol (15 mL). The suspension is centrifuged, and the combined organics are concentrated in vacuo. The residue is dissolved in methylene chloride (15 mL) and filtered using a syringe (0.45 micron filter) from the remaining inorganic salts. Concentration of the filtrates affords free tetrakis(aminomethyl)methane in a quantitative yield as a white semi-solid material (the residual alcohol is estimated by NMR). NMR (D2O) δ 2.9 (s, CH2)

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08900621B2uspto-grants-2014_12