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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325998Generated: November 1, 2026

Ethanol → Ethyl Acetate

https://huagongshe.com/reaction/325998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium ChlorideHCID 5234—
ReactantEthyl chloroacetateHCID 7751—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 178418416HCID 178418416—
SolventTolueneHCID 1140—
ProductEthyl chloroacetateHCID 7751—
ProductDiethyl MalonateHCID 7761—
ProductEthyl AcetateHCID 88571%

Reaction Conditions

Temperature55 °C

Reaction Steps

In a pressure vessel of a capacity of 7.5 liters, equipped with a pH measuring system, 20 g of Co2 (CO)8, 10 g of NaCl as conducting salt, and 2.5 liters of ethanol denatured with toluene are combined. The apparatus is scavenged three times with carbon monoxide, and then a CO pressure of 7.5 atmospheres gauge is established. While the vessel is heated at 55° C., a solution of 20.5% sodium ethylate in ethanol is pumped in from a reservoir by means of a proportioning pump such that a pH of 7 to 8 is reached, the liquid and gas phases being thoroughly mixed by means of a circulating pump. After the reaction temperature is reached, 490 g (4 moles) Of chloroacetic acid ethyl ester is proportioned into the vessel at a constant CO pressure of 8.0 at. gauge over a period of 15 minutes, and a 20.6% solution of sodium ethylate is added through a second inlet so as to maintain a pH of approximately 7.0. Over a period of 6 hours, 1.12 kg (3.4 moles) of 20.6% sodium ethylate is pumped in. Then the vessel is cooled, the pressure is relieved, and the vessel is purged with nitrogen. The reaction solution is separated from the sodium chloride on a suction filter and distilled. 517 g of malonic acid diethyl ester is obtained (95% yield), plus 2.5 g of acetic acid ethyl ester (approx. 1% yield) and 5 g of high-boiling compounds plus 73 g of chloroacetic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443624
Source datasetuspto-grants-1984_04
ORD IDord-173c42b622d94c21963a01bd10960989
Source noteuspto-grants-1984_04