Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | (2-tert-Butyl-6-methyl-4H-pyran-4-ylidene)propanedinitrile | HCID 15374739 | — |
| Reactant | HCID 18458012 | HCID 18458012 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 73446802 | HCID 73446802 | 48.8% |
Reaction Steps
As shown in the following reaction 1, 2.14 g (10 mmol) of 2-(2-tert-butyl-6-methyl-pyran-4-ylidene)-malononitrile and 2.13 g (10 mmol) of 7-dimethylamino-2,3-dihydro-thieno[3,4-b][1,4]dioxine-5-carbaldehyde were added into 100 ml of ethanol, and 0.93 g (11 mmol) of piperidine was added thereto. The reaction solution was heated at 75° C. for 10 hours. After cooling the reaction solution, the precipitated red solid was filtered, and recrystallized with ethanol to obtain 2 g of the target compound (Yield 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07211335B2 |
|---|
| Source dataset | uspto-grants-2007_05 |
|---|
| ORD ID | ord-8564b43dc7534184b7697101410e3e8d |
|---|
| Source note | uspto-grants-2007_05 |
|---|