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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848187Generated: October 25, 2026

Acetic Acid → Dimethyl 2-oxo-4-methyloctylphosphonate

https://huagongshe.com/reaction/848187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantHeptanoic acid, 3-methyl-, 1-methylpropyl esterHCID 85980—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductDimethyl 2-oxo-4-methyloctylphosphonateHCID 1301812184%

Reaction Conditions

Temperature-70 °C

Reaction Steps

Under an atmosphere of nitrogen, 375 ml of a 1.33 M solution of n-butyllithium in n-hexane were added dropwise to a solution of 61.9 g of dimethyl methylphosphonate in 587 ml of tetrahydrofuran at -70° C. After stirring the mixture for one hour at -70° C., a solution of 40 g of sec-butyl 3-methylheptanoate (prepared as described in Reference Example 1) in 70 ml of tetrahydrofuran was added dropwise at -70° C., and the mixture was stirred at the same temperature for 4 hours and then stirred overnight at room temperature. The reaction mixture was then acidified with acetic acid and filtered to remove the precipitated solid, and the filtrate was concentrated under reduced pressure. The residue was diluted with ethyl acetate, washed with water and a saturated aqueous solution of sodium chloride, dried over magnesium sulphate and concentrated under reduced pressure. The residue was purified by distillation under reduced pressure to give 42 g of the title compound having the following physical characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04294849
Source datasetuspto-grants-1981_10
ORD IDord-a7b691bee5f24488998202b3d4e00e59
Source noteuspto-grants-1981_10