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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387430Generated: November 1, 2026

Ethanol → ethyl 2-acetyl-3-ethoxybut-2-enoate

https://huagongshe.com/reaction/2387430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl AcetoacetateHCID 8868—
Reactant1,1-DiethoxyetheneHCID 137673—
CatalystSodium ethoxideHCID 2723922—
SolventEthyl AcetateHCID 8857—
Productethyl 2-acetyl-3-ethoxybut-2-enoateHCID 23147489%

Reaction Steps

A 5 L 4-neck flask equipped with a mechanical stirrer, condenser, thermowell, addition funnel and N2 inlet was charged with ethyl acetoacetate (493.1 g, 483 mL, 3.7931 mol, 1.0 equiv) and sodium ethoxide (3.1 g, 0.046 mol, 1.2 mol %). Ketene diethylacetal (880.0 g, 1000 mL, 7.5862 mol, 2.0 equiv) was added over 1 hr maintaining the reaction temperature at <22° C. by external cooling. When addition was complete, the reaction mixture was heated at 85° C.±5° C. for 7.5 hr. The yellow brown reaction mixture was cooled to room temperature and stirred overnight. Much of the lower boiling components [EtOH, EtOAc, Me(OEt)3] were stripped on a roto-evaporator (bath temperature 65° C.). The residual yellow-orange oil was distilled, collecting the fraction with bp 100-107° C. (1.8-2.1 Torr) to give 675.2 g (89%) of product as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268826B2
Source datasetuspto-grants-2012_09
ORD IDord-839fb2c47680487d8115d0a6b9e37204
Source noteuspto-grants-2012_09