HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 3-((5-(hydroxymethyl)furan-2-yl) methylene)-N-acetyl-2-oxoindoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 5-(Hydroxymethyl)furfural | HCID 237332 | — |
| Reactant | 1-Acetylindolin-2-one | HCID 323719 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-((5-(hydroxymethyl)furan-2-yl) methylene)-N-acetyl-2-oxoindoline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08053461B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-d681d2db206c4d6eadb06b44412df9dd |
| Source note | uspto-grants-2011_11 |