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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420489Generated: October 31, 2026

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

https://huagongshe.com/reaction/2420489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantPotassium CarbonateHCID 11430—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Indoleglyoxylyl chlorideHCID 89952—
ReactantPhenyl(piperidin-4-yl)methanoneHCID 226102—
SolventDiethyl EtherHCID 3283—
SolventChloroformHCID 6212—
Product1-(4-benzoyl-1-piperidyl)-2-(1H-indol-3-yl)ethane-1,2-dioneHCID 20311711—

Reaction Steps

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 1 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##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04110459
Source datasetuspto-grants-1978_08
ORD IDord-cd30f8827dc14a378d8e1bb5666cbae3
Source noteuspto-grants-1978_08