Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255810Generated: October 26, 2026

Didecylamine → N,N,N',N'-Tetradecyl-2-butene-1,4-diamine

https://huagongshe.com/reaction/2255810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDidecylamineHCID 14261—
Reactant2-Butene-1,4-diol diacetateHCID 140402—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductN,N,N',N'-Tetradecyl-2-butene-1,4-diamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240976
Source datasetuspto-grants-1993_08
ORD IDord-66487a77a77544d9a85bc971095cc37c
Source noteuspto-grants-1993_08