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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 73840Erstellt: 23. Oktober 2026

1-Aminocyclohexanecarboxylic acid → HCID 24740121, Verbindung

https://huagongshe.com/de/reaction/73840

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Aminocyclohexanecarboxylic acidHCID 1366—
EduktThionyl ChlorideHCID 24386—
EduktSodium BicarbonateHCID 516892—
Edukt5-Methylisoxazole-4-carboxylic acidHCID 1425240—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
ProduktHCID 24740121HCID 2474012116%

Reaktionsschritte

1 g (7.87 mmol) of 5-methylisoxazole-4-carboxylic acid was added to 3 ml of thionyl chloride, and the mixture was stirred overnight. Under reduced pressure, the reaction solution was concentrated, and the obtained residue was added to a solution of 1.13 g (7.87 mmol) of 1-aminocyclohexanecarboxylic acid and 6.6 g (79 mmol) of sodium hydrogencarbonate in 30 ml of toluene-30 ml of water. After the mixture was stirred at room temperature overnight, the toluene layer was separated. The aqueous layer was neutralized by potassium hydrogensulfate, and it was extracted with ethyl acetate. After the obtained organic layer was washed with saturated brine, it was dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, methylene chloride was added thereto, and under ice-cooling, 332 mg (1.73 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride was added. After the mixture was stirred at room temperature overnight, under reduced pressure, the reaction solution was concentrated, ethyl acetate was added thereto, and the mixture was successively washed with water, a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 295 mg (16%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829209B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-2a330b4be3674c6681db8055d377aa19
Quellennotizuspto-grants-2014_09