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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50380Erstellt: 26. Oktober 2026

Ethyl Thioglycolate → Ethyl 1-methyl-2-methoxymethylthieno[2,3-d]imidazol-5-yl-carboxylate

https://huagongshe.com/reaction/50380

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl ThioglycolateHCID 12185—
EduktSodium ethoxideHCID 2723922—
Edukt5-Chloro-4-formyl-2-methoxymethyl-1-methylimidazoleHCID 18412528—
LösungsmittelEthanolHCID 702—
ProduktEthyl 1-methyl-2-methoxymethylthieno[2,3-d]imidazol-5-yl-carboxylateHCID 18412470—

Reaktionsschritte

To a freshly prepared sodium ethoxide solution (from 391 mg, 17 mmol of sodium) in 15 mL of ethanol were added dropwise 1.9 mL (2.1 g, 17 mmol) of ethyl thioglycolate. After 1 hour stirring at ambient temperature, 1.6 g (8.5 mmol) of 5-chloro-4-formyl-2-methoxymethyl-1-methylimidazole in 20 mL of absolute ethanol were added and the mixture was heated to 80° C. (analogously to B. Iddon et al., J. Chem. Soc. Perkin Trans. I, 1987, 1457). After 5 hours, the solvent was distilled off, the residue was taken up in 50 mL of methylene chloride and washed with 20 mL of water. The aqueous phase was washed again with 20 mL of methylene chloride and then the combined organic phases were dried with sodium sulfate. After removal of the solvent in vacuo, the crude product obtained was purified by column chromatography (aluminium oxide; methylene chloride). Yield: 1.0 g (46% of theory), C11H14N2O3S (254.31); Rf value: 0.48 (silica gel; methylene chloride/ethanol=50:1); EKA mass spectrum: (M+H)+=255; (M+Na)+=277.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710055B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-8e3e094bc68e4b11aa81df298a8cdf45
Quellennotizuspto-grants-2004_03