HuagongsheHuagongshe Chemistry Print Report · For research reference only
Didecylamine → N,N,N',N'-Tetradecyl-2-butene-1,4-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Didecylamine | HCID 14261 | — |
| Reactant | 2-Butene-1,4-diol diacetate | HCID 140402 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N,N,N',N'-Tetradecyl-2-butene-1,4-diamine | HCID 54366770 | — |
Reaction Steps
A solution of di-n-decylamine (10.9 g, 36.6 mmol) and 2-butene-1,4-diol diacetate (3.15 g, 18.3 mmol) in tetrahydrofuran (THF) (150 ml) is treated with tetrakis(triphenylphosphine)palladium(0) (1.0 g, 0.9 mmol) and stirred at room temperature overnight. The reaction mixture is concentrated in vacuo to a oil that is redissolved in THF (500 ml) and treated with 20% aqueous sodium hydroxide (250 ml). The mixture is stirred for one hour, concentrated, and extracted with ether. The ether extracts are dried and concentrated giving an orange oil which is purified by medium pressure chromatography (silica gel; 25% ethyl acetate in hexanes). The title compound is isolated as 5.8 g (49% yield) of a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05391808 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-094180197c384a0788740ca7dd012497 |
| Source note | uspto-grants-1995_02 |