HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(5-Nitrofuran-2-yl)prop-2-enal → 5-Nitro-2-[(o-butylbenzoylhydrazono)propen-1-yl]furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(5-Nitrofuran-2-yl)prop-2-enal | HCID 15863 | — |
| Reactant | Butyl benzhydrazide | HCID 13157627 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Nitro-2-[(o-butylbenzoylhydrazono)propen-1-yl]furan | HCID 151572 | — |
Reaction Steps
A solution of 1.7 g of the butyl benzhydrazide mentioned under (4) above in 20 ml of dichloromethane is mixed with a solution of 3.5 g of 3-(5-nitro-2-furyl)acrylaldehyde in 20 ml of dichloromethane, and the mixture is stirred at room temperature. The yellow-brown product (precipitated after a reaction time of 3 hours) is sucked off, the filtrate is concentrated, and the resulting solid material is likewise isolated. The two precipitates are recrystallized together from 200 ml of ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04051253 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-162d43a5ac5543a8a6376e8feb8bc634 |
| Source note | uspto-grants-1977_09 |