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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1175192Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1175192

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropyleneHCID 8252—
EduktPotassium CarbonateHCID 11430—
EduktEpibromohydrinHCID 18430—
Edukt3,4-Dihydroxy-thiophene-2,5-dicarboxylic acid diethyl esterHCID 245503—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Hydroxymethyl-2,3-dihydrothieno[3,4-b][1,4]dioxine-5,7-dicarboxylic acid diethyl esterHCID 5929478755%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07838688B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-2b22a6db6a2743f1ba3da6325adcd093
Quellennotizuspto-grants-2010_11