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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22206Erstellt: 23. Oktober 2026

Diethyl Ether → HCID 178473683, Verbindung

https://huagongshe.com/de/reaction/22206

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktSodium hydrideHCID 24758—
EduktIodide IonHCID 30165—
EduktNeryl chlorideHCID 5874259—
EduktHCID 178473686HCID 178473686—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 178473683HCID 178473683—

Reaktionsschritte

To a stirred mixture of 123 mg (5.13 mmol) of sodium hydride in 10 mL of DMF at 0° C. under argon was added 1.32 g (5.13 mmol) of Example 1, Part A [(ethoxymethylphosphinyl)methyl]phosphonic acid, diethyl ester in 5 mL of DMF dropwise over 20 minutes. The mixture was stirred for 0.5 hours and was treated with 1.00 g (3.42 mmol) of Part A iodide in 3 mL of DMF. The reaction was stirred at 0° C. for 1 hour then at room temperature for 48 hours, at which time the reaction was diluted with ether and quenched with saturated NH4Cl. The organic layer was washed with water, brine, dried (MgSO4) and evaporated to provide 1.10 g of a pale yellow oil. Flash chromatography was performed on 100 g of silica gel eluted with 49.5:49.5:1 acetone/ethyl acetate/methanol (1 liter) followed by 45:45:10 acetone/ethyl acetate/methanol. Pure product fractions were combined and evaporated to provide 600 mg (43%) of title ester as a pale yellow oil, a mixture of diastereomers.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428028
Quelldatensatzuspto-grants-1995_06
ORD IDord-6a90e7ab0f284dfc9b059e1e2c7eb2d0
Quellennotizuspto-grants-1995_06