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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555665Generated: October 25, 2026

Piperidine → 3-((5-(hydroxymethyl)furan-2-yl) methylene)-N-acetyl-2-oxoindoline

https://huagongshe.com/reaction/555665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant5-(Hydroxymethyl)furfuralHCID 237332—
Reactant1-Acetylindolin-2-oneHCID 323719—
SolventEthanolHCID 702—
Product3-((5-(hydroxymethyl)furan-2-yl) methylene)-N-acetyl-2-oxoindolineHCID 66986626—

Reaction Steps

N-acetyloxindole (1 equivalent), 5-hydroxymethyl-2-furaldehyde (0.5 equivalent) and piperidine (0.2 equivalent) were dissolved in ethanol such that 1 mL of ethanol was used per 1 μmol of the total amount of the compounds, and the resulting mixture was stirred at room temperature for 12 hours. After completion of the reaction, the resulting precipitate was collected by filtration, washed with cooled ethanol several times and dried, whereby 3-((5-(hydroxymethyl)furan-2-yl) methylene)-N-acetyl-2-oxoindoline was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053461B2
Source datasetuspto-grants-2011_11
ORD IDord-d681d2db206c4d6eadb06b44412df9dd
Source noteuspto-grants-2011_11