HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 86749038, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | Cinnamaldehyde | HCID 637511 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86749038 | HCID 86749038 | — |
Reaction Steps
A solution of 11.2 g (0.1 mol) of 1,3-cyclohexanedione in 110 mL of ethanol was stirred at room temperature while 1 mL of piperidine was added followed by the dropwise addition of 13 mL (0.103 mol) of trans-cinnamaldehyde over a 2 min period. The resulting mixture was stirred at room temperature for 2 hr and then in an ice-bath for 1 hr. The resulting yellow slurry was filtered with suction and the solid dried under high vacuum giving 13.9 g (61.5%) of the title dione. Recrystallization of a sample of this material from ethyl acetate gave yellow solid, mp 115.5°-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05457124 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-8bbe25bb56c5402481f1f90c68e8c36f |
| Source note | uspto-grants-1995_10 |