Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860885Generated: October 26, 2026

Piperidine → 5-acetyl-3-(1H-indol-2-ylmethylene)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1860885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantIndole-2-carboxaldehydeHCID 96389—
Reactant5-acetyl-2,3-dihydro-1H-indol-2-oneHCID 10219643—
SolventEthanolHCID 702—
Product5-acetyl-3-(1H-indol-2-ylmethylene)-1,3-dihydro-indol-2-oneHCID 5435871088%

Reaction Steps

A mixture of 5-acetyl-2-oxindole (88 mg), indole-2-carbaldehyde (87 mg) and piperidine (4 mg) in ethanol (2 mL) was held in a sealed tube at 90° C. for 3 hours. The mixture was cooled to room temperature. The solid which formed was collected by vacuum filtration, washed with cold ethanol and dried in a vacuum oven to give 133 mg (88% yield) of 5-acetyl-3-(1H-indol-2-ylmethylene)-1,3-dihydro-indol-2-one as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531502B1
Source datasetuspto-grants-2003_03
ORD IDord-a7c5c1417d754ee1b31afd6a17290d4d
Source noteuspto-grants-2003_03