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HRID 16717Erstellt: 24. Oktober 2026

1,2-Ethanediamine, N1,N1,N2-trimethyl- → HCID 178501159, Verbindung

https://huagongshe.com/de/reaction/16717

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktSodium BicarbonateHCID 516892—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktHCID 178501163HCID 178501163—
LösungsmittelChloroformHCID 6212—
ProduktHCID 178501159HCID 17850115993,3%

Reaktionsschritte

Trans-4-(methoxycarbonyl)cyclohexanecarboxylic acid (8.84 g) obtained in Reference Example 1(2) is dissolved in chloroform (100 ml), and thereto are added 1-hydroxybenzotriazole (7.14 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (10.00 g) and N,N,N′-trimethylethylenediamine (5.33 g) under ice-cooling. The mixture is then stirred at room temperature for 4 hours. Saturated aqueous sodium hydrogen carbonate solution is poured to the reaction solution and the mixture is extracted with chloroform. The organic layer is washed with saturated brine and dried over sodium sulfate. The solvent is concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography (eluent: chloroform/methanol/28% ammonia water=200/10/1) to give methyl trans-4-{[[2-(dimethylamino)ethyl](methyl)amino]carbonyl}-cyclohexanecarboxylate (11.98 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737161B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-8b58af24ecdb470eb2de945d1ee82651
Quellennotizuspto-grants-2010_06