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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1728953Erstellt: 26. Oktober 2026

Hydrochloric Acid → HCID 178470333, Verbindung

https://huagongshe.com/reaction/1728953

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium ChlorideHCID 5234—
EduktDiethyl OxalateHCID 7268—
EduktPotassium thiocyanateHCID 516872—
EduktSodiumHCID 5360545—
Eduktethyl 2-(N-phenylformamido)acetateHCID 14416604—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktHCID 178470333HCID 17847033348%

Reaktionsschritte

Absolute ethanol (50 mL) was slowly added to a mechanically stirred suspension of finely cut sodium metal (19.3 g; 0.84 mol) in anhydrous ether (500 mL). When most of the metal had dissolved, diethyl oxalate (114 mL; 0.84 mol) was slowly added followed by the slow addition of the N-phenyl-N-formylglycine ethyl ester (130 g; 0.67 mol). The mixture was stirred at room temperature overnight and then ice-water (700 mL) was added. The resulting emulsion was broken by sequential addition of a saturated sodium chloride solution (150 mL) and water (200 mL). The aqueous layer was removed, potassium thiocyanate (114 g; 1.18 mol) was added, then concentrated hydrochloric acid (160 mL), followed by absolute ethanol (900 mL). The resultant mixture was warmed at 60°-65° C. for 1 hour, then at 50° C. for 6 hours and finally allowed to stir at room temperature overnight. The light yellow precipitate was filtered, washed with ethanol and dried to give 103 g (48%) of diethyl 2-mercapto-1-phenyl-4,5-imidazoledicarboxylate (mp 145°-146° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05329012
Quelldatensatzuspto-grants-1994_07
ORD IDord-1706884c5fd742b48f17201e467f3009
Quellennotizuspto-grants-1994_07