反応 #1483083
ord-f41422ae8c9e4910bda7808b0388f11a
反応方程式
溶媒
反応条件
後処理
- 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その他A 50 mL flask is equipped with a reflux condenser and a magnetic stirrer
- 3温度refluxed for 4 hours
- 4温度cooled
- 5その他Methanol solution is decanted from the inorganic salts
- 6濃縮the combined organics are concentrated in vacuo
- 7workup.DISSOLUTIONThe residue is dissolved in methylene chloride (15 mL)
- 8ろ過filtered
- 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)