Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 736039Erstellt: 24. Oktober 2026

Sodium Iodide → Diethyl 2-(trifluoromethyl)benzylphosphonate

https://huagongshe.com/de/reaction/736039

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktTriethyl phosphiteHCID 31215—
Edukt1-(Chloromethyl)-2-(trifluoromethyl)benzeneHCID 89028—
LösungsmittelAcetonitrileHCID 6342—
ProduktDiethyl 2-(trifluoromethyl)benzylphosphonateHCID 15818095—

Reaktionsschritte

To a suspension of sodium iodide (3.85 g, 25.6 mmol, 1 equiv.) in acetonitrile at room temperature under argon is added neat 1-chloromethyl-2-trifluoromethyl-benzene (commercially available from Acros Organics USA). To the resulting milky suspension is added freshly distilled triethyl phosphite (4.26 g, 25.6 mmol, 1 equiv.) and the resulting solution is stirred overnight at room temperature. After that time further triethyl phosphite (2.13 g, 12.9 mmol, 0.5 equiv.) is added and the reaction mixture heated at reflux for 1 hour. After cooling down to room temperature all volatiles were evaporated under reduced pressure. The residue is taken-up in dichloromethane and filtered through paper and the filtrate is concentrated under reduced pressure to yield the desired material as a clear oil pure enough to be used in the following step without further purification (7.46 g, 98%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07595315B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-866ca2e02fe7473f80b86807ac5b81a6
Quellennotizuspto-grants-2009_09