HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 2-(1-Acetylpiperidin-4-yl)propenal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylazanium;chloride | HCID 12954980 | — |
| Reactant | HCID 21468226 | HCID 21468226 | — |
| Product | 2-(1-Acetylpiperidin-4-yl)propenal | HCID 45119214 | — |
Reaction Steps
3.95 g (23.3 mmol) of 2-(1-acetylpiperidin-4-yl)ethanol, 2.12 g (26.3 mmol) of dimethylammonium chloride and 3 ml (40 mmol) of 37% formaldehyde solution are heated at 110° C. for 2 hours with stirring. The mixture is allowed to cool and is extracted several times with diethyl ether. The organic phases are combined, washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and concentrated to dryness by evaporation. 2-(1-acetylpiperidin-4-yl)propenal is obtained in the form of a yellowish oil which can be further reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05488140 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-22529da802a84b0abbec516a97fb4203 |
| Source note | uspto-grants-1996_01 |