تفاعل #1483083

ord-f41422ae8c9e4910bda7808b0388f11a

معادلة التفاعل

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

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTetrakis(aminomethyl)methane is prepared by a known procedure (Adil, K. et al., Solid State Sciences, 6 (2004), 1229-1235)
  2. 2
    أخرىA 50 mL flask is equipped with a reflux condenser and a magnetic stirrer
  3. 3
    درجة الحرارةrefluxed for 4 hours
  4. 4
    درجة الحرارةcooled
  5. 5
    أخرىMethanol solution is decanted from the inorganic salts
  6. 6
    تركيزthe combined organics are concentrated in vacuo
  7. 7
    workup.DISSOLUTIONThe residue is dissolved in methylene chloride (15 mL)
  8. 8
    ترشيحfiltered
  9. 9
    ترشيح(0.45 micron filter) from the remaining inorganic salts

الإجراء التجريبي

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)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08900621B2uspto-grants-2014_12