Reaction #1435700
ord-8564b43dc7534184b7697101410e3e8d
Reaction equation
piperidine
2-(2-tert-butyl-6-methyl-pyran-4-ylidene)-malononitrile
7-dimethylamino-2,3-dihydro-thieno[3,4-b][1,4]dioxine-5-carbaldehyde
→
target compound
Yield 48.8%
2-{2-tert-butyl-6-[2-(7-dimethylamino-2,3-dihydro-thieno[3,4-b][1,4]dioxine-5-yl)-vinyl]-pyran-4-ylidene}-malononitrile
Yield 48.8%
Reactants
Reagents
None
Solvents
Conditions
Temperature
75°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1workup.ADDITIONwas added
- 2TemperatureAfter cooling the reaction solution
- 3Filtrationthe precipitated red solid was filtered
- 4Otherrecrystallized with ethanol
Procedure
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%).