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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 727494Erstellt: 24. Oktober 2026

Diethyl chlorophosphate → Isopropyl (Diethoxyphosphoryl)methanesulfonate

https://huagongshe.com/de/reaction/727494

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl chlorophosphateHCID 13139—
EduktIsopropyl methanesulfonateHCID 13551—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktIsopropyl (Diethoxyphosphoryl)methanesulfonateHCID 1572597567%

Reaktionsbedingungen

Temperatur-40 °C

Reaktionsschritte

To a rapidly stirred solution of 8.28 g (60 mmol) of isopropyl methanesulfonate in 150 mL of THF at -73° C. (internal temp.) was added 25 mL (60 mmol) of 2.4M n-butyllithium dropwise over 20 min. The internal temperature was not allowed to rise above -69° C. throughout the course of the addition. After an additional 15 min., 5.17 g (30 mmol) of freshly distilled diethyl chlorophosphate was added at a rate to keep the solution temperature below -69° C. The reaction mixture was stirred for 0.3 h at -73° C. and for 0.5 h at -40° C. when it was quenched with 125 mL of saturated NH4Cl solution. The reaction mass was warmed to room temperature and the THF removed under reduced pressure. The remainder was partitioned between methylene chloride and water (3×75 mL). The extracts were dried (Na2SO4), concentrated, and purified by flash chromatography (350 g silica gel) eluting with 1:1 methylene chloride/ether to provide 5.20 g (67%) of title compound as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05712396
Quelldatensatzuspto-grants-1998_01
ORD IDord-595cfc84a1e44c3f97b7e9e63e460877
Quellennotizuspto-grants-1998_01