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HRID 270640作成日:2026年10月26日

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

https://huagongshe.com/reaction/270640

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl 3-oxoglutarateHCID 74591—
反応物Lithium BromideHCID 82050—
反応物1,4-Dithiane-2,5-diolHCID 98330—
溶媒1,4-DioxaneHCID 31275—
生成物Methyl 2-(2-methoxy-2-oxoethyl)thiophene-3-carboxylateHCID 5895296382.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07449580B2
出典データセットuspto-grants-2008_11
ORD IDord-e0ca6cd818a64c73aa1634761220ada2
出典メモuspto-grants-2008_11