HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362818Generated: October 30, 2026
Malononitrile → [4-(2-Azidoethoxy)benzylidene]malononitrile
https://huagongshe.com/reaction/2362818
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-(2-Azidoethoxy)benzaldehyde | HCID 17922552 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [4-(2-Azidoethoxy)benzylidene]malononitrile | HCID 86624335 | — |
Reaction Steps
47 μl (0.47 mmol) of piperidine are added dropwise to a solution of 3.02 g (15.79 mmol) of the compound from Example 36A and 1.09 g (16.42 mmol) of malonodinitrile in 100 ml of ethanol, and the reaction mixture is stirred at +78° C. for 3.5 h. During this time, the colour of the solution changes to orange-red. After cooling to RT, the solution is allowed to stand without stirring for 20 h. A colourless precipitate is formed. Using a rotary evaporator, the crude suspension is concentrated to half of its original volume, and the crystallization is completed with cooling in an ice bath. The resulting precipitate is filtered off with suction and washed twice with in each case 20 ml of ethanol and twice with in each case 20 ml of methyl tert-butyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691850B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-b94ffd6381404fde9236d265cd0fd221 |
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| Source note | uspto-grants-2014_04 |
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