Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1719377Erstellt: 26. Oktober 2026

Hydrochloric Acid → 1-(5-Carboxypentyl)-2-(1-imidazolyl)-3-methylindole hydrochloride

https://huagongshe.com/reaction/1719377

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
Edukt1-(5-Methoxycarbonylpentyl)-2-(1-imidazolyl)-3-methylindoleHCID 13280840—
LösungsmittelEthanolHCID 702—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1-(5-Carboxypentyl)-2-(1-imidazolyl)-3-methylindole hydrochlorideHCID 20268194—

Reaktionsschritte

A mixture of 1-(5-methoxycarbonylpentyl)-2-(1-imidazolyl)-3-methylindole (1.80 g) and 30 ml of 3N NaOH is stirred at room temperature for 1.3 hours. The resulting clear, yellow solution is neutralized to pH 6 with 2N HCl. The resulting suspension is extracted with ethyl acetate (2×50 ml). The organic extract is washed with a saturated NaCl solution (1×25 ml), dried (MgSO4), filtered, and concentrated in vacuo to give a cream-colored solid. The solid is dissolved in ethanol and the solution treated with 0.6 ml of 6.5N HCl in ethanol. The solution is diluted with diethyl ether and after standing for several hours the precipitate which forms is collected by filtration to give 1-(5-carboxypentyl)-2-(1-imidazolyl)-3-methylindole hydrochloride, m.p. 177.5°-180.5° decomposition.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04539410
Quelldatensatzuspto-grants-1985_09
ORD IDord-90188c2ea98f4ed7b689613b8d334c9a
Quellennotizuspto-grants-1985_09