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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 505910Erstellt: 27. Oktober 2026

Hydrochloric Acid → HCID 178468758, Verbindung

https://huagongshe.com/reaction/505910

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-NitrobenzaldehydeHCID 541—
EduktEthyl 2,3-diaminobenzoateHCID 11171330—
EduktSodium sulfide monohydrateHCID 19906495—
KatalysatorCupric acetateHCID 8895—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktHCID 178468758HCID 178468758—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

1.5 g (8.3 mmol) of ethyl 2,3-diaminobenzoate and 1.1 ml of concentrated acetic acid were dissolved in 50 ml of methanol. 1.6 g (10.8 mmol) of 4-nitrobenzaldehyde, dissolved in 150 ml of methanol, were then added dropwise over a period of 30 minutes. 2.2 g (10.8 mmol) of copper(II) acetate, dissolved in 100 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 3 ml of 32% strength hydrochloric acid were added. This was followed by careful dropwise addition of a solution of 3.1 g of sodium sulfide hydrate in 50 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 2.2 g of the intermediate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07781596B1
Quelldatensatzuspto-grants-2010_08
ORD IDord-9b83b6de3022465da82d947610961d9c
Quellennotizuspto-grants-2010_08