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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22448Generated: October 27, 2026

Sodium ethoxide → Sodium ethoxide

https://huagongshe.com/reaction/22448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantSodiumHCID 5360545—
Reactant(2S)-4-Methyl-2-sulfanylpentanoic acidHCID 13633259—
SolventEthanolHCID 702—
ProductSodium ethoxideHCID 2723922—
Product2-Mercapto-4-Methylpentanoic AcidHCID 13633258—
Product(2S)-4-Methyl-2-sulfanylpentanoic acidHCID 13633259—

Reaction Steps

A 0.43 M solution of sodium ethoxide (Solution A) was prepared with freshly cut sodium and anhydrous ethanol. An ethanol solution of Compound 1, (S)-2-mercapto-4-methylpentanoic acid (0.72 g in 25 mls), (solution B), was prepared. A 13.5 ml volume of solution A was slowly added to 15 ml of solution B under nitrogen atmosphere. The solution was stirred for five minutes, and the ethanol removed in vacuo, and the white solid repeatedly evaporated with benzene until dry. The resulting disodium salt of mercaptoleucine was dissolved in ~1 ml of dimethylsulfoxide (DMSO) to which was added 1.58 g of compound 2 dissolved in 2 mls of DMSO, and stirred overnight. The reaction mixture was combined with 175 ml of distilled water and extracted with 20 ml portions of ether three times and then acidified with 5N HCl with stirring at 0° C. The aqueous solution was re-extracted 3X with ethyl acetate. The extract was washed with a saturated NaCl solution and dried over sodium sulfate, filtered, and the ethyl acetate removed in vacuo yielding 1.05 g of a clear oil. This was crystallized from ethyl acetate and hexane; yielding a white solid; (0.83 g), (mp, 110-111), ([.varies.]25=52.5 (C0.88 l, MeoH)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428019
Source datasetuspto-grants-1995_06
ORD IDord-1970afc9aa89468fa5acca20061cf090
Source noteuspto-grants-1995_06