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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 877074Erstellt: 24. Oktober 2026

Benzylamine → 1-Benzyl-4-methyl-1,4-azaphosphinane 4-oxide

https://huagongshe.com/de/reaction/877074

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzylamineHCID 7504—
EduktTetrahydrofuranHCID 8028—
EduktMethyl phosphonic dichlorideHCID 12671—
EduktAmmonium ChlorideHCID 25517—
EduktHCID 178461836HCID 178461836—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-Benzyl-4-methyl-1,4-azaphosphinane 4-oxideHCID 6683324651%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a vigorously stirred solution of methylphosphonic dichloride (6.65 g, 50 mmol) in THF (100 mL) at −78° C. was added vinylmagnesium chloride (1.6 M in THF, 66 mL, 105 mmol) dropwisely over 30 min. After the addition is completed, the reaction mixture was warmed to 0° C. over 1 hour, and to it was added benzylamine (6.43 g, 60 mmol) and methanol (100 mL). The reaction mixture was then refluxed for 36 hours. After cooled to room temperature, the reaction mixture was poured into a separation funnel containing saturated aqueous ammonium chloride (100 mL), ethyl acetate (200 mL) and water (100 mL). The organic layer was separated, and the aqueous layer was extracted with methylene chloride (100 mL) twice. The combined organic layer and extracts were dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography, eluting with 20% methanol in dichloromethane to give the desired product as white crystalline solid (5.69 g, 51%). LCMS ESI(+) m/z: 224 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08987284B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-dc8905d3763642f3bbc4290eadcfc9d6
Quellennotizuspto-grants-2015_03