HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-{4-[2-Amino-3,5-dicyano-6-(phenylsulphanyl)-4-pyridinyl]phenyl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(4-(2,2-Dicyanoethenyl)phenyl)acetamide | HCID 33296 | — |
| Reactant | 2-Hydroxybutanedinitrile | HCID 21253562 | — |
| Product | N-{4-[2-Amino-3,5-dicyano-6-(phenylsulphanyl)-4-pyridinyl]phenyl}acetamide | HCID 12016387 | — |
Reaction Steps
318 g (1.5 mol) of N-[4-(2,2-dicyanovinyl)phenyl]acetamide, 99 g (1.5 mol) of malonitrile and 166 g (1.5 mol) of thiophenol are initially introduced in 2 000 ml of ethanol, and 6.7 ml of triethylamine are then added. The mixture is stirred under reflux for 2 hours, in connection with which crystallization takes place. After the mixture has cooled down to room temperature, the product is filtered off with suction and dried in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07045631B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-475cce6f5d1c4c04b1b150097e163411 |
| Source note | uspto-grants-2006_05 |