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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464353Generated: November 2, 2026

Acetic Acid → HCID 178471403, compound

https://huagongshe.com/reaction/1464353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantIsobutyl iodideHCID 10556—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178472265HCID 178472265—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 178471403HCID 17847140344%

Reaction Conditions

Temperature10 °C

Reaction Steps

12.0 g of diethyl 2-[(acetamido)(hydroxyphosphinyl)methyl]malonate were dissolved in 100 ml of dry dimethyl sulphoxide and the solution was cooled to 10° C. while stirring under a nitrogen atmosphere. 3.2 g of 60% sodium hydride in mineral oil were added, the mixture was stirred at room temperature for 2 hours and then 8 g of isobutyl iodide were added. The mixture was stirred at room temperature in the dark for 20 hours and 20 ml of glacial acetic acid were added. The volatiles were removed by evaporation in a high vacuum and the resulting semi-solid residue was dissolved in 100 ml of water containing 15 ml of 50% hypophosphorous acid. The solution was extracted eight times with ethyl acetate and the combined extracts were dried over sodium sulfate and evaporated. The residue was dissolved in dichloromethane and the solution was washed in sequence with water and saturated sodium chloride solution. The dichloromethane solution was dried over sodium sulfate and evaporated, and the residue was crystallized from diethyl ether/n-hexane to give 6.28 g of diethyl 2-[(acetamido)-(hydroxyphosphinyl)methyl]-2-isobutylmalonate in the form of a white solid; MS: 352 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05304549
Source datasetuspto-grants-1994_04
ORD IDord-bf6b2388142f42f9bfe4eedeabb014b8
Source noteuspto-grants-1994_04