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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 981178Erstellt: 26. Oktober 2026

Triethylamine → Sodium 5-phenyl-4,5-dihydro-1H-pyrazole-1-carboxylate

https://huagongshe.com/reaction/981178

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl chloroformateHCID 10928—
EduktSodium HydroxideHCID 14798—
Edukt5-Phenyl-4,5-dihydro-1H-pyrazoleHCID 120841—
LösungsmittelEthanolHCID 702—
LösungsmittelChloroformHCID 6212—
ProduktSodium 5-phenyl-4,5-dihydro-1H-pyrazole-1-carboxylateHCID 23690231—

Reaktionsschritte

Ethyl chloroformate (12 g) was added dropwise under ice cooling to a solution of 14.6 g 5-phenyl-2-pyrazoline and 12 g triethylamine in 100 ml chloroform, and the mixture was stirred at room temperature for three hours. The reaction mixture was washed with 3% hydrochloric acid and 3% aqueous solution of sodium bicarbonate in that order and then dried over anhydrous sodium sulfate. The solvent was distilled off from the dried solution, and the oily residue thus obtained (20 g) was dissolved in 80 ml ethanol. To this ethanolic solution, was added 10 ml of 40% aqueous solution of caustic soda, the mixture was stirred at room temperature for one hour, and the crystals which precipitated out were collected by filtration and dried under reduced pressure, affording 12 g of pure product. M.p.: 210° C. (dec.); NMR (D2O): 2.6-3.4 (2H, m), 4.7 (1H, dd, J=12,5 Hz), 7.14 (1H, t, J=2 Hz), 7.40 (5H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04990529
Quelldatensatzuspto-grants-1991_02
ORD IDord-d7876466e5f5473dae08da8b048ca086
Quellennotizuspto-grants-1991_02