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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867752Generated: October 25, 2026

Acetic Acid → Dimethyl (3-methyl-2-oxobutyl)phosphonate

https://huagongshe.com/reaction/867752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl isobutyrateHCID 11039—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl (3-methyl-2-oxobutyl)phosphonateHCID 1262854788%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Dimethyl methylphosphonate (8.8 g, 0.071 mol) was dissolved in anhydrous THF (100 ml) under argon atmosphere. To the solution stirred at -78° C. was added dropwise n-butyl lithium (1.58N, 45 ml, 0.071 mol) over 30 minutes and then a solution of methyl isobutyrate (2.9 g, 0.0284 mol) in anhydrous THF (5 ml) was added dropwise over 30 minutes. The reaction mixture was warmed to room temperature. After 30 minutes, acetic acid (4.3 ml) and water (10 ml) were added with ice cooling. After concentration, water (20 ml) was added to the residue and the mixture was extracted with ethyl acetate (50 ml×2). The ethyl acetate layers were washed with water (20 ml×1) and with brine (20 ml×1), dried over anhydrous sodium sulfate, and concentrated. Distillation of the residue gave dimethyl 3-methyl-2-oxo-butylphosphonate (4.8 g, 0.025 mol, yield 88%, b.p.= 82°-84° C./0.31 mmHg). The structure was identified by the following data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04775692
Source datasetuspto-grants-1988_10
ORD IDord-7b5c12fddb154797b17ba72cd4a46851
Source noteuspto-grants-1988_10