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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1606579Erstellt: 25. Oktober 2026

CID 406 → Dimethyl 2-oxo-undecylphosphonate

https://huagongshe.com/reaction/1606579

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCID 406HCID 406—
EduktMethyl DecanoateHCID 8050—
EduktDimethyl methylphosphonateHCID 12958—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
ProduktDimethyl 2-oxo-undecylphosphonateHCID 10612624—

Reaktionsschritte

A solution of 49.6 g. (0.40 mole) dimethyl methylphosphonate (Aldrich) in 500 ml. dry tetrahydrofuran is cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution is added 188 ml. of 2.34 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 40 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 36.3 g. (0.20 mole) methyl decanoate is added dropwise at a rate that kept the reaction temperature less than -70° (20 minutes). After 1.0 hour at -78° the reaction mixture is allowed to warm to ambient temperature, neutralized with 25 ml. acetic acid and rotary evaporated to a white gel. The gelatinous material is taken up in 75 ml. water, the aqueous phase extracted with 100 ml. portions of chloroform (3x), the combined organic extracts are backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, to give dimethyl 2-oxo-undecylphosphonate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03953466
Quelldatensatzuspto-grants-1976_04
ORD IDord-dd1dd85ce54b4e2e8e59589fd180eae7
Quellennotizuspto-grants-1976_04