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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595070Generated: October 26, 2026

Ethyl Thioglycolate → Ethyl 4-[(2-ethoxy-2-oxoethyl)thio]butanoate

https://huagongshe.com/reaction/595070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ThioglycolateHCID 12185—
ReactantEthyl 4-chlorobutyrateHCID 18474—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductEthyl 4-[(2-ethoxy-2-oxoethyl)thio]butanoateHCID 277884795.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium metal (4.3 g, 0.18 mol) was added cautiously in small portions to ethanol (150 mL). After the sodium completely dissolved, the mixture was cooled to 0° C. and ethyl 2-sulfanylacetate (21.9 g, 0.18 mol), was added. Ethyl 4-chlorobutanoate (27.4 g, 0.18 mol) was then added slowly and the resulting mixture stirred overnight at rt. The solid was filtered off, and then the filtrate concentrated under reduced pressure. The oil obtained was partitioned between water and ethyl acetate. The organic layer was collected, dried over anhydrous Na2SO4 and concentrated under vacuum to give the desired ethyl 4-((ethoxycarbonyl)methylthio)butanoate (40.2 g, 95%) as colorless oil. The crude material was used without further purification in the follow step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242993B2
Source datasetuspto-grants-2016_01
ORD IDord-38879612a4614b2f9eb66bbcecbe9b03
Source noteuspto-grants-2016_01