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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 505912Erstellt: 26. Oktober 2026

Hydrochloric Acid → HCID 178468757, Verbindung

https://huagongshe.com/reaction/505912

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-(1H-imidazol-1-yl)benzaldehydeHCID 736530—
EduktEthyl 2,3-diaminobenzoateHCID 11171330—
EduktSodium sulfide monohydrateHCID 19906495—
KatalysatorCupric acetateHCID 8895—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktHCID 178468757HCID 178468757—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

1 g (5.5 mmol) of ethyl 2,3-diaminobenzoate and 0.7 ml of concentrated acetic acid were dissolved in 13 ml of methanol. 1.24 g (7.2 mmol) of 4-imidazol-1-ylbenzaldehyde, dissolved in 25 ml of methanol, were then added dropwise over a period of 30 minutes. 1.4 g (7.2 mmol) of copper(II) acetate, dissolved in 19 ml of warm water, were then rapidly added dropwise, and the entire mixture was subsequently refluxed for 20 minutes. The reaction solution was cooled to 50° C. and 2.25 ml of 32% strength hydrochloric acid were added. This was followed by careful dropwise addition of a solution of 2.13 g of sodium sulfide hydrate in 15 ml of water, and the entire mixture was stirred for another 15 minutes. The reaction solution was poured into ice-water and the resulting precipitate was filtered off with suction. The filtrate was made alkaline using aqueous sodium bicarbonate solution and extracted repeatedly with ethyl acetate. The ethyl acetate phase was separated off, dried and concentrated under reduced pressure. This gave 1.7 g of the intermediate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07781596B1
Quelldatensatzuspto-grants-2010_08
ORD IDord-dab53d02ab754cfbaa0a787a6ae807b6
Quellennotizuspto-grants-2010_08