HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 73446801, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | (2-tert-Butyl-6-methyl-4H-pyran-4-ylidene)propanedinitrile | HCID 15374739 | — |
| Reactant | 5-[4-(Diphenylamino)phenyl]thiophene-2-carbaldehyde | HCID 18458010 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 73446801 | HCID 73446801 | 50% |
Reaction Steps
As shown in the following reaction 3, 0.72 g (3.37 mmol) of (2-(2-tert-butyl-6-methyl-pyran-4-ylidene)-malononitrile and 1 g (2.81 mmol) of 5-(4-diphenylamino-phenyl)-thiophene-2-carbaldehyde were added into 50 ml of ethanol, and 0.28 g (3.37 mmol) of piperidine was added thereto. The reaction solution was heated for 24 hours while refluxing. After cooling the reaction solution, the precipitated red solid was filtered, and recrystallized with ethanol to obtain 0.79 g of the target compound (Yield 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07211335B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-dd590dc6069b484bbd50972ff09490a8 |
| Source note | uspto-grants-2007_05 |