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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582410Generated: November 2, 2026

Ethylene Glycol → Diethyl 2,3-dihydrothieno[3,4-b][1,4]dioxine-5,7-dicarboxylate

https://huagongshe.com/reaction/1582410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant3,4-Dihydroxy-thiophene-2,5-dicarboxylic acid diethyl esterHCID 245503—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl 2,3-dihydrothieno[3,4-b][1,4]dioxine-5,7-dicarboxylateHCID 62539995.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

ADC01 (2.9 g, 16.9 mmol) was slowly added to a solution of 3,4-dihydroxythiophene-2,5-dicarboxylic acid diethyl ester (2.0 g, 7.7 mmol), ethylene glycol (0.5 g, 8.5 mmol), and PHOL (3.4 g, 16.9 mmol) in dry tetrahydrofuran (150 ml) at 25° C. The reaction mixture was stirred for 3 h and then refluxed for 9 h. The reaction mixture was allowed to cool to 25° C. and concentrated by rotary evaporator to remove the THF. The residue was diluted with diethyl ether and allowed to stand overnight to enable the tributylphosphine oxide to precipitate out. The tributylphosphine oxide was then removed by filtration and the residue purified by chromatography on silica gel (eluant: ethyl acetate/ hexane=2/1) to give 2.1 g of 2,3-dihydro-thieno[3,4-b][1,4]dioxine-5,7-dicarboxylic acid diethyl ester as white crystals (95% yield) as fully characterized by 1H NMR, 13C NMR, HRMS, and elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734312B2
Source datasetuspto-grants-2004_05
ORD IDord-893932b2e0e04472ae811988e4540847
Source noteuspto-grants-2004_05