HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862039Generated: October 29, 2026
Piperidine → 2-(4-pyridylmethylene) indan-1,3-dione
https://huagongshe.com/reaction/1862039
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1,3-Indandione | HCID 11815 | — |
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Product | 2-(4-pyridylmethylene) indan-1,3-dione | HCID 2732731 | — |
Reaction Steps
A mixture of indane-1,3-dione (5.85 g), piperidine (0.46 ml) and pyridine-4-carboxaldehyde (4.31 g) was stirred in IMS (40 ml) at ambient temperature for 50 minutes. The mixture was cooled in an ice-bath but no crystallization occurred. The solution was allowed to warm to ambient temperature and then the solvent was removed under reduced pressure to give a residue which was partially purified by flash column chromatography on silica using 10% industrial methylated spirit in dichloromethane followed by 20% industrial methylated spirit in dichloromethane as the mobile phases. The leading fractions were collected, combined and evaporated to give a solid which was triturated with ice-cold diethyl ether and filtered to give 2-(4-pyridylmethylene) indan-1,3-dione, m.p. 152-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06534655B1 |
|---|
| Source dataset | uspto-grants-2003_03 |
|---|
| ORD ID | ord-abbee2548d7c4919923cc24560c5c654 |
|---|
| Source note | uspto-grants-2003_03 |
|---|