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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270640Generated: October 25, 2026

Dimethyl 3-oxoglutarate → Methyl 2-(2-methoxy-2-oxoethyl)thiophene-3-carboxylate

https://huagongshe.com/reaction/270640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl 3-oxoglutarateHCID 74591—
ReactantLithium BromideHCID 82050—
Reactant1,4-Dithiane-2,5-diolHCID 98330—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 2-(2-methoxy-2-oxoethyl)thiophene-3-carboxylateHCID 5895296382.4%

Reaction Steps

100.0 g of dimethyl 1,3-acetonedicarboxylate was dissolved in 2,800 ml of dioxane, and added thereto were 52.5 g of 2,5-dihydroxy-1,4-dithiane and 5.0 g of lithium bromide. The resulting mixture was refluxed for 15 hours, cooled to room temperature, and concentrated by evaporation. To the residue, 1,000 ml of n-hexane was added, stirred, and the hexane layer was separated. This extraction procedure was repeated twice using 500 ml portions of n-hexane. The separated n-hexane layers were combined and concentrated under reduced pressure to obtain 60.9 g (yield of 49%) of the title compound as an oil, which was directly used in the next step without any purification. An analytical sample of the title compound could be obtained by vacuum distillation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449580B2
Source datasetuspto-grants-2008_11
ORD IDord-e0ca6cd818a64c73aa1634761220ada2
Source noteuspto-grants-2008_11