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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352336Generated: November 2, 2026

Sodium ethoxide → HCID 86743472, compound

https://huagongshe.com/reaction/2352336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
ReactantHCID 14651684HCID 14651684—
SolventEthanolHCID 702—
ProductHCID 86743472HCID 86743472—

Reaction Steps

A solution of 123.1 g (0.38 mol, 2.5% less than theory) of "21 weight percent sodium ethoxide in ethanol" (Aldrich Chemical Co.) is added all at once to a solution of 101 g (0.39 mol) of (S)-2-[(3-ethoxy-1,3-dioxopropyl)amino]-4-methylpentanoic acid, methyl ester in 200 ml of absolute ethanol. There is no heat of reaction. After about two minutes a solid separates (sodium salt of product) and the mixture becomes thick. The mixture is heated at reflux for 30 minutes (complete solution) and then cooled to room temperature (solid reappears). The solid is collected by filtration and washed with diethyl ether. The resulting cake is dissolved by adding to 1 L of ice water with stirring, 400 ml of 1 N hydrochloric acid solution is added and the separated solid is filtered, washed with water and dried one hour under suction to afford (S)-2,5-dihydro-4-hydroxy-5-(2-methylpropyl)-2-oxo-1H-pyrrole-3-carboxylic acid, ethyl ester as a moist solid which is used in the next steps without further purification. TLC (acetic acid, methanol, chloroform, silica gel, iodine) Rf =0.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04876343
Source datasetuspto-grants-1989_10
ORD IDord-c39a97dafd7748a3b768485735d6da7a
Source noteuspto-grants-1989_10