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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973343Generated: October 29, 2026

Potassium Iodide → Diethyl 2-(5-acetoxypentyl)-2-methylmalonate

https://huagongshe.com/reaction/973343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantDimethylformamideHCID 6228—
ReactantDiethyl methylmalonateHCID 11857—
ReactantSodium hydrideHCID 24758—
Reactant3-CHLOROPHENYL ACETATEHCID 83061—
ProductDiethyl 2-(5-acetoxypentyl)-2-methylmalonateHCID 54079282—

Reaction Steps

Sodium hydride (4.8 g., 0.2 mole) as a 50% suspension in mineral oil is washed with petroleum ether under nitrogen to remove the mineral oil, suspended in dry benzene (150 ml.), and the suspension cooled in an ice bath. Diethyl methylmalonate (34.8 g., 0.2 mole) dissolved in sieve dried DMF (150 ml.) is added to the suspension of sodium hydride dropwise. The mixture is allowed to stand overnight at room temperature. Potassium iodide (0.4 g.) and 5-acetoxyphenyl chloride (32.9 g., 0.2 mole) are then added, and the mixture is heated for 24 hours at 125° in an oil bath. The reaction mixture is concentrated in vacuo, diluted with ether (200 ml.), and filtered to remove sodium chloride. The filtrate is washed with brine, dried over anhydrous magnesium sulfate and concentrated to yield 39.6 g. (66%) of oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04055597
Source datasetuspto-grants-1977_10
ORD IDord-9a80df9c3e55467d8d15e0734c6ecf9a
Source noteuspto-grants-1977_10