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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857799Generated: October 31, 2026

Ethylenediamine → N-[3,5-bis(trifluoromethyl)benzyl]ethylenediamine

https://huagongshe.com/reaction/1857799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantThionyl ChlorideHCID 24386—
Reactant[3,5-Bis(trifluoromethyl)phenyl]methyl methanesulfonateHCID 18387265—
Reactant2-Chloro-4-phenylnicotinic acidHCID 18387312—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductN-[3,5-bis(trifluoromethyl)benzyl]ethylenediamineHCID 18387337—

Reaction Steps

Thionyl chloride (0.15 ml) and DMF (catalytic amount) were added to a THF (5 ml) solution of 2-chloro-4-phenyl-3-pyridinecarboxylic acid (145 mg) and heated under reflux for 2 hours. The solvent was removed by distillation, and the residue was dissolved in THF (5 ml). The resulting solution was added to a mixture of N-[3,5-bis(trifluoromethyl)benzyl]-N'-tert-butoxycarbonylethylenediamine (240 mg), triethylamine (0.26 ml) and THF (10 ml), while cooling with ice, and stirred for 3 hours at room temperature. The N-[3,5-bis(trifluoromethyl)benzyl]-N'-tert-butoxycarbonylethylenediamine used herein was prepared as an oily compound, by reacting ethylenediamine with 3,5-bis(trifluoromethyl)benzyl methanesulfonate in THF to give an oily compound of N-[3,5-bis(trifluoromethyl)benzyl]ethylenediamine, followed by further reacting the compound with di-tert-butyl dicarbonate in the presence of triethylamine in THF.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147071
Source datasetuspto-grants-2000_11
ORD IDord-e1f864373e784c9a91a240d1639194f3
Source noteuspto-grants-2000_11