HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Nitrothiophene-2-carboxaldehyde → HCID 67582692, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Nitrothiophene-2-carboxaldehyde | HCID 78281 | — |
| Reactant | Sulphonyl diacetonitrile | HCID 142163 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67582692 | HCID 67582692 | — |
| Product | HCID 88414059 | HCID 88414059 | — |
Reaction Steps
A mixture of (0.5 g) of 2-nitrothiophen-5-carboxaldehyde and (0.7 g) of sulfonyl diacetonitrile in 6 mL ethanol was refluxed with a few drops of piperidine for 4 hours. Ethanol was removed in a rotavap and the mixture worked up with ethylacetate, diluted acid and brine. A portion of the crude was then purified by HPLC on a C-18 column to provide (0.05 g) of (E)-2-cyanomethylsulfonyl-3-(2-nitrothien-5-yl)acrylonitrile along with (0.03 g) of (E,E)-2-[[1-cyano-2-(2-nitrothien-5-yl)ethenyl]sulfonyl]-3-(2-nitrothien-5-yl)acrylonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05710173 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-3dcc6fd963ca4a3b83425bf6b2ba5022 |
| Source note | uspto-grants-1998_01 |