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HRID 1175192作成日:2026年10月27日

Propylene → 2-Hydroxymethyl-2,3-dihydrothieno[3,4-b][1,4]dioxine-5,7-dicarboxylic acid diethyl ester

https://huagongshe.com/reaction/1175192

反応式

関与物質

役割名称HCID仕込み量
反応物PropyleneHCID 8252—
反応物Potassium CarbonateHCID 11430—
反応物EpibromohydrinHCID 18430—
反応物3,4-Dihydroxy-thiophene-2,5-dicarboxylic acid diethyl esterHCID 245503—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒HexaneHCID 8058—
溶媒Ethyl AcetateHCID 8857—
生成物2-Hydroxymethyl-2,3-dihydrothieno[3,4-b][1,4]dioxine-5,7-dicarboxylic acid diethyl esterHCID 5929478755%

反応手順

7.7 mL (0.0902 mol) of epibromohydrin and 1.92 g (0.0139 mol) of potassium carbonate were dissolved in 100 mL water and added to a refluxing mixture of 16.11 g (0.0694 mol) diethyl 3,4-dihydroxythiophene-2,5-dicarboxylate in 350 mL ethanol. After heating to reflux for 1 hour, an additional 5.3 mL (0.0624 mol) epibromohydrin was added and the reaction heated to reflux overnight. Upon cooling to room temperature the reaction was concentrated by evaporation and then poured into 500 ml water. The mixture was acidified and then extracted with methylene chloride until the organic wash no longer indicated product was present. The organic fractions were washed with saturated brine then dried with magnesium sulfate. The solvent was removed under reduced pressure to give a yellow solid. Column chromatography was performed using 60% ethyl acetate in hexane to give a 70:30 mixture of the product and propylene isomer in 55% yield as a white solid. Structure and purity were confirmed by 1H/13C NMR and LC-MS.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07838688B2
出典データセットuspto-grants-2010_11
ORD IDord-2b22a6db6a2743f1ba3da6325adcd093
出典メモuspto-grants-2010_11