Sodium methanolate methanol → 4742-00-1

HRID 1425608Notes

Reaction equation

HRID 1425608 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-63e572a3ba3845388427c9cb8c484f50
Source dataset
uspto-grants-2015_01
Patent number
US08932638B2

Reaction notes

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