Sodium methanolate methanol → 4742-00-1
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
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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
- customTetrakis(aminomethyl)methane is prepared by a known procedure (Adil, K. et al., Solid State Sciences, 6 (2004), 1229-1235)
- customA 50 mL flask is equipped with a reflux condenser and a magnetic stirrer
- temperaturerefluxed for 4 hours
- temperaturecooled
- customMethanol solution is decanted from the inorganic salts
- concentrationthe combined organics are concentrated in vacuo
- dissolutionThe residue is dissolved in methylene chloride (15 mL)
- filtrationfiltered
- 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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