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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625029Generated: October 30, 2026

Acetic Acid → HCID 12710774, compound

https://huagongshe.com/reaction/625029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 2777633HCID 2777633—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 12710774HCID 12710774100%

Reaction Steps

A three neck flask was charged with NaOEt (21%, 200 mL, 537 mmol) in ethanol. The solvent was removed under vacuum and to the residue was added toluene (500 mL). The mixture was heated to reflux and methyl 3-(2-methoxy-2-oxoethylthio)butanoate (92 g, 446 mmol) was added dropwise. After addition was complete, the mixture was refluxed for 4 hours. After cooling, the mixture was poured into a mixture of acetic acid (200 g) and crushed ice (200 g). The mixture was stirred overnight and then diluted with ethyl acetate (500 mL). The organic phase was separated and washed with saturated Na2CO3 and brine and then dried. The solvent was removed to afford crude methyl 2-methyl-4-oxo-tetrahydrothiophene-3-carboxylate (77.7 g, 99%). 1H NMR (CDCl3, 400 MHz) δ 11.23-11.15 (d, 1H), 7.27-7.16 (m, 2H), 4.33-4.12 (m, 2H), 3.95-3.68 (m, 2H). 3.60-3.15 (m, 1H), 2.60-2.20 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303040B2
Source datasetuspto-grants-2016_04
ORD IDord-0ae258a73a4748489e81a2cab93e9741
Source noteuspto-grants-2016_04