Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459741Generated: October 29, 2026

Triethylamine → HCID 15907546, compound

https://huagongshe.com/reaction/459741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(4-Nitrophenyl)butyric acidHCID 79711—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 68579243HCID 68579243—
ReactantHCID 178418300HCID 178418300—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 15907546HCID 1590754684%

Reaction Steps

4-(N-methylpiperazinyl)aniline (0.5 g; 2.6 mmol), hydroxybenzotriazole (0.39 g; 2.86 mmol), 1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride (1.1 g; 5.7 mmol) and triethylamine (0.8 ml; 5.7 mmol) are added to a solution of 0.55 g (2.6 mmol) of 4-(4-nitrophenyl)butanoic acid in dichloromethane (30 ml). The reaction medium is stirred for 16 hours at ambient temperature, then the medium is diluted with 15 ml of water and the product is extracted with dichloromethane. The organic phase is dried over sodium sulphate followed by filtering and concentrating under vacuum and the residue is purified on a silica column (eluent: CH2Cl2/EtOH: 4/1). A clear oil is obtained with a yield of 84% (0.84 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196084B2
Source datasetuspto-grants-2007_03
ORD IDord-b41610da23d04c1baa346187642f635e
Source noteuspto-grants-2007_03