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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 247694Erstellt: 24. Oktober 2026

Dicyclohexylcarbodiimide → HCID 178444551, Verbindung

https://huagongshe.com/de/reaction/247694

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt4-EthoxyphenolHCID 12150—
EduktHCID 178444555HCID 178444555—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178444551HCID 17844455183,5%

Reaktionsschritte

A mixture of 520 mg of trans-4-(4-pentenyl)cyclohexanecarboxylic acid, 439.4 mg of p-ethoxyphenol, 765.5 mg of dicyclohexylcarbodiimide and 45 mg of 4-(dimethylamino)pyridine were dissolved in 80 ml of methylene chloride and the solution was stirred at room temperature for 20 hours. Subsequently, the reaction mixture was diluted with diethyl ether, the precipitated urea was filtered off and the filtrate was concentrated. The residue was taken up in hexane and the solution was washed with dilute hydrochloric acid, sodium hydrogen carbonate solution and water. The aqueous phases were back-extracted twice with hexane. The organic phases were dried over magnesium sulphate and evaporated. Low-pressure chromatography of the resulting residue on silica gel with ethyl acetate/petroleum ether (vol. 3:97) gave an 0.7 g (83%) of trans-4-(4-pentenyl)cyclohexanecarboxylic acid p-ethoxyphenyl ester. After recrystallization from 3 ml of methanol there were finally obtained 455 mg of product in the form of colourless crystals; m.p. (C-N) 32.7° C., cl.p. (N-I) 57.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04709030
Quelldatensatzuspto-grants-1987_11
ORD IDord-88d42fa00ec645d7b222c81884225647
Quellennotizuspto-grants-1987_11