HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitroaniline → 2-Cyano-3-(methylthio)-3-((4-nitrophenyl)amino)acrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Reactant | 2-Cyano-3,3-bis(methylthio)acrylamide | HCID 2747746 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Cyano-3-(methylthio)-3-((4-nitrophenyl)amino)acrylamide | HCID 86701867 | — |
Reaction Steps
Dissolved 10.00 g 2-cyano-3,3-bis(methylthio)acrylamide in 100 mL of ethanol. Then added 7.337 g (1.00 eq.) of 4-nitroaniline to the reaction vessel and stirred the reaction at 75° C. until starting amide was absent and confirmed by HPLC. Once complete (18 hrs), the reaction was brought to room temperature and filtered to obtain 2-cyano-3-(methylthio)-3-((4-nitrophenyl)amino)acrylamide as an off white to light yellow powder as product. The product was allowed to dry under vacuum for 1 hr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346792B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-ed8535276b4b4e4a89dfb4e799999d01 |
| Source note | uspto-grants-2016_05 |