HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → (E)-1-(3,5-Dimethoxyphenyl)-3-(indol-3-yl)-2-propen-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Indole-3-Carboxaldehyde | HCID 10256 | — |
| Reactant | 1-(3,5-Dimethoxyphenyl)ethan-1-one | HCID 95997 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (E)-1-(3,5-Dimethoxyphenyl)-3-(indol-3-yl)-2-propen-1-one | HCID 21850309 | 95.4% |
Reaction Steps
3',5'-Dimethoxyacetophenone (1.10 g) and indole-3-carboxaldehyde (1.45 g) were dissolved in ethanol (20 ml), and piperidine (0.85 g) was added thereto, followed by heating under reflux for 32 hours. The reaction solution was cooled to room temperature, and the precipitated crystals were collected by filtration, followed by recrystallization from ethanol to give Compound 69 (1.79 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05952355 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-14f4bd9d7ada40209b16df0cc3b1eae8 |
| Source note | uspto-grants-1999_09 |