HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → (4-(Trifluoromethyl)benzyl)malononitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | (4-(Trifluoromethyl)benzylidene)malononitrile | HCID 714296 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | (4-(Trifluoromethyl)benzyl)malononitrile | HCID 10656743 | 51,3% |
Reaktionsschritte
First, 4.44 g of (4-(trifluoromethyl)benzylidene)malononitrile was dissolved in 20 ml of ethanol, and while stirring at room temperature, a suspension of 0.19 g of sodium borohydride in 5 ml of ethanol was added dropwise, followed by stirring at room temperature for 30 minutes. Then, 10% hydrochloride acid was added to the reaction mixture, which became acidic and was extracted with diethyl ether. The organic layer was successively washed with 10% hydrochloric acid, a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 2.30 g of (4-(trifluoromethyl)benzyl)malononitrile (the intermediate (4)).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07402691B2 |
| Quelldatensatz | uspto-grants-2008_07 |
| ORD ID | ord-d8439fc2695e4fb0b52aae099c3403eb |
| Quellennotiz | uspto-grants-2008_07 |