HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → (4-(Trifluoromethylthio)benzyl)malononitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | 4-(Trifluoromethylthio)benzylidenemalononitrile | HCID 22234975 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (4-(Trifluoromethylthio)benzyl)malononitrile | HCID 22234991 | 77.1% |
Reaction Steps
Then, 8.00 g of (4-(trifluoromethylthio)benzylidene)malononitrile and 3.35 g of benzaldehyde were dissolved in 320 ml of ethanol, and while stirring at room temperature, 3.41 g of phenylenediamine was slowly added, and the mixture was stirred at room temperature for 5 hours. Then, the reaction mixture was concentrated, 300 ml of t-butyl methyl ether was added, and insoluble matters were filtered. The filtrate was concentrated and the resulting residue was subjected to silica gel chromatography to give 6.22 g of (4-(trifluoromethylthio)benzyl)malononitrile (the intermediate (14)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07402691B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-9fb9eccb93004b279213118abb35b9b5 |
| Source note | uspto-grants-2008_07 |