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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 893205Erstellt: 24. Oktober 2026

Triethylamine → Ethyl 1-(4-chloro-2-ethylphenylaminocarbonyl)cyclopropanecarboxylate

https://huagongshe.com/de/reaction/893205

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl chloroformateHCID 10928—
Edukt4-Chloro-2-ethylanilineHCID 34871—
Edukt1-(Ethoxycarbonyl)cyclopropanecarboxylic acidHCID 11789472—
LösungsmittelAcetonitrileHCID 6342—
ProduktEthyl 1-(4-chloro-2-ethylphenylaminocarbonyl)cyclopropanecarboxylateHCID 1909684940%

Reaktionsschritte

To a stirred solution of 1.54 grams (0.01 mole) of 1-carboethoxycyclopropanecarboxylic acid (the monocarboxylic acid intermediate described in Example XVIII) and 0.99 gram (0.01 mole) of triethylamine in 75 milliliters of acetonitrile was added a solution of 1.06 grams (0.01 mole) of ethyl chloroformate in 25 milliliters of acetonitrile dropwise with cooling to 0° C.-5° C. After stirring at ice temperature for 30 minutes a solution of 1.52 grams (0.01 mole) of 4-chloro-2-ethylaniline in 20 milliliters of acetonitrile was fed dropwise with stirring and continued cooling. The reaction mixture was allowed to warm to room temperature, then stirred for approximately sixteen hours following which it was filtered and the filtrate freed of solvent by evaporation. The residue was dissolved in dichloromethane and extracted, successively, with water (2×50 milliliters), 2N HCl (2×50 milliliters) and water (1×50 milliliters). After drying (MgSO4), solvent was removed by evaporation and the solid recrystallized from hexane to give 1.15 grams (0.004 mole) of ethyl 1-(4-chloro-2-ethylphenylaminocarbonyl)cyclopropanecarboxylate as cream colored prisms having a melting point of 77° C.-80° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05123951
Quelldatensatzuspto-grants-1992_06
ORD IDord-f370e5f079d2420890f13c7d8f75c678
Quellennotizuspto-grants-1992_06