Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5185Erstellt: 24. Oktober 2026

Benzyl Bromide → Ethyl 2-benzyl-2-cyanoethyl(diethoxymethyl)phosphinate

https://huagongshe.com/de/reaction/5185

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktDiisopropylamineHCID 7912—
EduktAmmonium ChlorideHCID 25517—
EduktEthyl 2-cyanoethyl(diethoxymethyl)phosphinateHCID 10037677—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktEthyl 2-benzyl-2-cyanoethyl(diethoxymethyl)phosphinateHCID 14362814—

Reaktionsschritte

To a solution of 0.97 g of diisopropylamine in 40 ml of tetrahydrofuran at -78° C. under an atmosphere of nitrogen are added 6.0 ml of a 1.6M solution of n-butyllithium in hexane. This solution is then stirred for a period of 10 minutes at this temperature, after which time a solution of 2.0 g of ethyl 2-cyanoethyl(diethoxymethyl)phosphinate in 10 ml of tetrahydrofuran is added. This mixture is then stirred for a period of 1 hour at -78° C. after which time a solution of 1.4 g of benzyl bromide in 10 ml of tetrahydrofuran is introduced. This mixture is then allowed to warm to room temperature when 40 ml of a saturated ammonium chloride solution is added. The aqueous layer is then extracted with 2×25 ml of diethyl ether and the organic extracts are combined and dried over magnesium sulphate. The solvent is then evaporated under reduced pressure and the crude product chromatographed on silica gel using ethyl acetate as an eluent to give ethyl 2-benzyl-2-cyanoethyl(diethoxymethyl)phosphinate as a viscous oil, 31P=+40.7 and +40.5 ppm (CDCl3).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05243062
Quelldatensatzuspto-grants-1993_09
ORD IDord-856eab2a0560410681b793d4b1b773fd
Quellennotizuspto-grants-1993_09