Sodium methanolate methanol → 4742-00-1

HRID 1773101Notes

Reaction equation

HRID 1773101 reaction equation
[Cl-].[Cl-].[Cl-].[Cl-].[NH2:5][CH2:6][C:7]([CH2:12][NH2:13])([CH2:10][NH2:11])[CH2:8][NH2:9].C[O-].[Na+].CO>CO>[NH2:5][CH2:6][C:7]([CH2:12][NH2:13])([CH2:10][NH2:11])[CH2:8][NH2:9]

Participants

4

Procedure

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)

Workup

  1. customTetrakis(aminomethyl)methane is prepared by a known procedure (Adil, K. et al., Solid State Sciences, 6 (2004), 1229-1235)
  2. customA 50 mL flask is equipped with a reflux condenser and a magnetic stirrer
  3. temperaturerefluxed for 4 hours
  4. temperaturecooled
  5. customMethanol solution is decanted from the inorganic salts
  6. concentrationthe combined organics are concentrated in vacuo
  7. dissolutionThe residue is dissolved in methylene chloride (15 mL)
  8. filtrationfiltered
  9. filtration(0.45 micron filter) from the remaining inorganic salts

Sources & evidence

ORD record
ord-5c059a6c95594d0a92ec211cdc0e7f53
Source dataset
uspto-grants-2016_02
Patent number
US09254334B2

Reaction notes

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