Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389029Generated: November 1, 2026

Acetic Acid → Dimethyl 2-oxo-2-phenylethylphosphonate

https://huagongshe.com/reaction/1389029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCID 406HCID 406—
ReactantTetrahydrofuranHCID 8028—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductDimethyl 2-oxo-2-phenylethylphosphonateHCID 56947329%

Reaction Steps

A solution of 74.5 g (600 mmoles) dimethyl methylphosphonate (Aldrich) in 750 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution was added 265 ml of 2.34 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 30 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 41 g (300 mmole) of methyl azoate was added dropwise at a rate that kept the reaction temperature less than -70° (10 minutes). After 1 hour at -78° the reaction mixture was allowed to warm to ambient temperature, neutralized with 35 ml acetic acid and rotary evaporated to a white gel. The gelatinous material was taken up in 75 ml water, the aqueous phase extracted with 300 ml portions of ether (3x), the combined organic extracts were backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, b.p. 130°-5° (0.04 mm) to give 35 g (29%) dimethyl 2-oxo-2-phenylethylphosphonate (2a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04243595
Source datasetuspto-grants-1981_01
ORD IDord-4b59926ac9f946be84dceb54d7de561d
Source noteuspto-grants-1981_01