Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683216Generated: October 25, 2026

Bis(3-aminopropyl)amine → Bis(3-{[(4-methylphenyl)sulfonyl]amino}propyl)[(4-methylphenyl)sulfonyl]amine

https://huagongshe.com/reaction/1683216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(3-aminopropyl)amineHCID 5942—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
SolventPyridineHCID 1049—
ProductBis(3-{[(4-methylphenyl)sulfonyl]amino}propyl)[(4-methylphenyl)sulfonyl]amineHCID 37379759%

Reaction Steps

To a stirred solution of p-toluenesulfonyl chloride (240 g, 1.26 mole) in pyridine (600 ml) at 0° C. was added a solution of 1,5,9-triazanonane (50.0 g, 0.381 mole) in pyridine (100 ml) under a dry nitrogen atmosphere, maintaining the temperature <60° C. The addition required 15 minutes. The solvent was removed in vacuo and the resulting yellow oil was dissolved in ethyl acetate (1 l) and H2O (500 ml). The ethyl acetate layer was separated, washed with 0.1 N HCl, H2O and saturated NaCl solution and dried (MgSO4). The solution was decolorized with silica gel and the solvent was removed in vacuo to give 133 g (59% yield) of the crude product as a glassy solid: 1H NMR (CDCl3) δ 1.71 (quint, J=6.6 Hz, 4H), 2.42 (s, 6H), 2.43 (s, 3H), 2.96 (quart, J=6.4 Hz, 4H), 3.11 (t, J=6.8 Hz, 4H), 5.12 (t, J=6.6 Hz, 2H), 7.30 (m, 6H), 7.63 (m, 2H), 7.73 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637578
Source datasetuspto-grants-1997_06
ORD IDord-0f7d522247134c62a39e281e6b3f0436
Source noteuspto-grants-1997_06