HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2,3-Difluorobenzaldehyde → (NE,R)-N-[(2,3-difluorophenyl)methylidene]-2-methylpropane-2-sulfinamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2,3-Difluorobenzaldehyde | HCID 137664 | — |
| Edukt | tert-Butylsulfinamide, (R)-(+)- | HCID 10964479 | — |
| Katalysator | Copper Sulfate | HCID 24462 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | (NE,R)-N-[(2,3-difluorophenyl)methylidene]-2-methylpropane-2-sulfinamide | HCID 89479281 | 93% |
Reaktionsbedingungen
| Temperatur | 55 °C |
|---|
Reaktionsschritte
To a oven dried round bottom flask with stir bar was added 2,3-difluorobenzaldehyde (0.5 g, 3.52 mmol), (R)-2-methylpropane-2-sulfinamide (0.469 g, 3.87 mmol) and DCE (7.04 mL). To this mixture was then added Copper (II) Sulfate (0.842 g, 5.28 mmol). Reaction mixture heated in a preheated oil bath to 55° C. for 24 hours. The reaction mixture was filtered through a celite pad washing solids with DCE. Combined filtrate was concentrated to afford a viscous yellow oil of (R,E)-N-(2,3-difluorobenzylidene)-2-methylpropane-2-sulfinamide (0.8007 g, 3.26 mmol, 93% yield). LCMS m/z 246.1 (M+H)+, Rt 0.91 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08957068B2 |
| Quelldatensatz | uspto-grants-2015_02 |
| ORD ID | ord-b4868a9dcf0e4ea894954e678ea02149 |
| Quellennotiz | uspto-grants-2015_02 |