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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773101Generated: November 2, 2026

Sodium methanolate methanol → Save 3D Zoom 2,2-Bis(aminomethyl)-1,3-propanediamine

https://huagongshe.com/reaction/1773101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanolate methanolHCID 23694274—
ReactantHCID 86646412HCID 86646412—
SolventMethanolHCID 887—
ProductSave 3D Zoom 2,2-Bis(aminomethyl)-1,3-propanediamineHCID 3017969—

Reaction Steps

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)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09254334B2
Source datasetuspto-grants-2016_02
ORD IDord-5c059a6c95594d0a92ec211cdc0e7f53
Source noteuspto-grants-2016_02