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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 866996Erstellt: 25. Oktober 2026

Indole → 1-(4-benzoyl-1-piperidyl)-2-(1H-indol-3-yl)ethane-1,2-dione

https://huagongshe.com/reaction/866996

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndoleHCID 798—
EduktPotassium CarbonateHCID 11430—
EduktOxalyl chlorideHCID 65578—
Edukt3-Indoleglyoxylyl chlorideHCID 89952—
EduktPhenyl(piperidin-4-yl)methanoneHCID 226102—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelChloroformHCID 6212—
Produkt1-(4-benzoyl-1-piperidyl)-2-(1H-indol-3-yl)ethane-1,2-dioneHCID 20311711—

Reaktionsschritte

A sample of an indole of the formula ##STR7## in a solvent such as anhydrous ether is allowed to react with oxalyl chloride at a temperature of from -15° to 15° C. for from a couple of minutes to one hour to produce a mixture of a corresponding 3-indoleglyoxyloyl chloride in the solvent which is then added to a cooled solution of 4-benzoylpiperidine in a suitable organic solvent such as chloroform optionally containing an acid scavenger such as potassium carbonate and allowing the mixture to react at a temperature of from 15° to 40° C. for a few minutes to 12 hours to produce a 4-benzoyl-1-(indol-3-ylglyoxyloyl)piperidine of the formula ##STR8##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04101663
Quelldatensatzuspto-grants-1978_07
ORD IDord-dc7ca59438ab48e38566a4526c4c79c1
Quellennotizuspto-grants-1978_07