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HRID 12890Erstellt: 24. Oktober 2026

2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl ester → HCID 178470003, Verbindung

https://huagongshe.com/de/reaction/12890

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Propenoic acid, 2-cyano-3-ethoxy-, ethyl esterHCID 78943—
EduktSodium AcetateHCID 517045—
EduktHydrazino-cyclohexanol hydrochlorideHCID 67020953—
LösungsmittelEthanolHCID 702—
ProduktHCID 178470002HCID 178470002—
ProduktHCID 178470003HCID 17847000328%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

Hydrazino-cyclohexanol hydrochloride (1.920 g, 9.79 mmol) was dissolved in hot ethanol and then cooled slightly. Ethyl (ethoxymethylene)-cyanoacetate (1.520 g, 8.98 mmol) and anhydrous sodium acetate (2.013 g, 24.54 mmol) were added and the mixture was heated at 70° C. for 15 hours. After cooling to room temperature, the mixture was partitioned between methylene chloride and water. The aqueous phase was washed with a second portion of methylene chloride. The two organic phases were combined, washed with brine, dried over sodium sulfate and concentrated. Flash chromatography, eluting with a 0-20% methanol/ethyl acetate gradient, separated a large portion of the cis-trans mixture of isomers. After chromatography, pure fractions of each isomer were combined and crystallized from EtOAc-hexanes to give 5-amino-1-(cis-4-hydroxy-cyclohexyl)-1H-pyrazole-4-carboxylic acid ethyl ester (0.511 g, 23% (crop 1); 0.121 g, 5% (crop 2)) and 5-amino-1-(trans-4-hydroxy-cyclohexyl)-1H-pyrazole-4-carboxylic acid ethyl ester (0.625 g, 28%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728029B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-b0eb15d1b2804e658d0348c324e84c96
Quellennotizuspto-grants-2010_06