HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Phenylprop-2-Enal → (E,E)-2-(3,4-Dihydroxybenzylaminocarbonyl)-3-styrylacrylonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Phenylprop-2-Enal | HCID 307 | — |
| Reactant | HCID 178511180 | HCID 178511180 | — |
| Product | (E,E)-2-(3,4-Dihydroxybenzylaminocarbonyl)-3-styrylacrylonitrile | HCID 10267983 | — |
Reaction Steps
The compound was prepared as described in Example 3 by adding cinnamaldehyde (0.018 ml, 0.14 mmol) to N-(cyanoacetyl)3,4-dihydroxybenzylamide (Example 2, 0.03 g, 0.14 mmol). Afer refluxing for 2 h and recrystallization from ethanol, a yellow solid was obtained (0.027 g, 59%). The product gave the following analytical data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06800659B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-d62972da37b146e2b9ef40f8ee23fed8 |
| Source note | uspto-grants-2004_10 |