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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258814Generated: October 26, 2026

Acetic Acid → Dimethyl-2-oxo-3-phenylpropyl phosphonate

https://huagongshe.com/reaction/258814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCID 406HCID 406—
ReactantTetrahydrofuranHCID 8028—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductDimethyl-2-oxo-3-phenylpropyl phosphonateHCID 1280588429%

Reaction Steps

A solution of 6.2 g (50 mmoles) dimethyl methylphosphonate (Aldrich) in 125 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution was added 21 ml of 2.37 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 18 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 7.5 g (50.0 mmole) methyl was added dropwise at a rate that kept the reaction temperature less than -70° (20 minutes). After 3.5 hours at -78° the reaction mixture was allowed to warm to ambient temperature, neutralized with 6 ml acetic acid and rotary evaporated to a white gel. The gelatonous material was taken up in 75 ml water, the aqueous phase extracted with 100 ml portions of chloroform (3x), the combined organic extracts were backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, b.p. 134°-5° (<0.1 mm) to give 3.5 g (29%) dimethyl 2-oxo-3-phenylpropylphosphonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04035360
Source datasetuspto-grants-1977_07
ORD IDord-32fd69083278472ab32cc006ab113678
Source noteuspto-grants-1977_07