HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 9997363, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Indole-3-Carboxaldehyde | HCID 10256 | — |
| Reactant | [(1H-Indol-3-yl)methylidene]propanedinitrile | HCID 269623 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Product | HCID 9997363 | HCID 9997363 | 75% |
Reaction Steps
2-(Indol-3-ylmethylene)-malononitrile: A yellow suspension of malononitrile (0.114 g, 1.72 mmol), anhydrous EtOH (1.72 mL), indole-3-carboxaldehyde (0.250 g, 1.72 mmol), and piperidine (6.8 μL, 0.069 mmol) was heated to form a yellow solution. Within 5 min, a yellow precipitate was formed and the reaction mixture was cooled to room temperature over 15 min. The yellow precipitate was filtered and collected, yielding 0.250 g (75%) of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07528164B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-e2553fedb72d448792b3dc49d9e92aec |
| Source note | uspto-grants-2009_05 |