Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Benzenamine, 4-(phenylmethyl)- | HCID 136914 | — |
| Reactant | 2-Cyano-3,3-bis(methylthio)acrylamide | HCID 2747746 | — |
| Product | HCID 178513711 | HCID 178513711 | — |
Reaction Steps
Dissolved 0.500 g 2-cyano-3,3-bis(methylthio)acrylamide in 15 mL EtOH and added 4-Aminodiphenylmethane (1.0 eq.). Stirred reaction at 75° C. until starting amide was absent by HPLC. Once complete (18 hrs), reaction was brought to room temperature and filtered to obtain a light yellow powder as product. Product was allowed to dry under vacuum for 1 hr. Product was then suspended in 10 mL EtOH and hydrazine hydrate (1 eq.) was added dropwise. Reaction was heated at 75° C. until intermediate was absent (HPLC). Once intermediate was absent (18 hrs), reaction was brought to room temperature and filtered to obtain a yellow powder as product. 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-bc11d42c35ba4107ae816ba4cea3cdc3 |
|---|
| Source note | uspto-grants-2016_05 |
|---|