HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Nitrophenyl)prop-2-enal → (E,E)-2-(3,4-Dihydroxybenzylaminocarbonyl)-3-(4-nitrostyryl)acrylonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Nitrophenyl)prop-2-enal | HCID 15614 | — |
| Reactant | HCID 178511180 | HCID 178511180 | — |
| Product | (E,E)-2-(3,4-Dihydroxybenzylaminocarbonyl)-3-(4-nitrostyryl)acrylonitrile | HCID 9947247 | — |
Reaction Steps
The compound was prepared as described in Example 3 by adding 4-nitrocinnamaldehyde (0.009 g, 0.05 mmol) to N-(cyanoacetyl)3,4-dihydroxybenzylamide (Example 2, 0.010 g, 0.05 mmol). After refluxing for 2 h and recrystallization from ethanol a yellow solid was obtained (0.007 g, 39%). 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-db425cebb19a4301a6647668f8c97cf4 |
| Source note | uspto-grants-2004_10 |