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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53977Erstellt: 23. Oktober 2026

Sodium hydride → Ethyl 3-(5-bromobenzo[b]thien-2-yl)-2-ethoxycarbonyl-2-(4-methoxyphenyl)propionate

https://huagongshe.com/de/reaction/53977

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
EduktDiethyl 2-(4-methoxyphenyl)malonateHCID 2785178—
Edukt5-Bromo-2-(bromomethyl)benzo[b]thiopheneHCID 14819352—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl 3-(5-bromobenzo[b]thien-2-yl)-2-ethoxycarbonyl-2-(4-methoxyphenyl)propionateHCID 2184420292,4%

Reaktionsschritte

14.2 g of ethyl 2-ethoxycarbonyl-2-(4-methoxyphenyl)acetate was dissolved in 150 ml of tetrahydrofuran. 2.6 g of sodium hydride (oil type, 60%) was added to the above solution while stirring under ice cooling, and the stirring was continued for 20 minutes. To this was further added 17.2 g of 5-bromo-2-bromomethylbenzo[b]thiophene. After stirring at room temperature for 18 hours, the resulting reaction solution was mixed with ammonium chloride aqueous solution, and then extracted with ethyl acetate. After drying to distill off the solvent, the resulting residue was subjected to silica gel column chromatography using chloroform as an elution solvent, thereby obtaining 24.2 g of ethyl 3-(5-bromobenzo[b]thien-2-yl)-2-ethoxycarbonyl-2-(4-methoxyphenyl)propionate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05620991
Quelldatensatzuspto-grants-1997_04
ORD IDord-dbde7cd1490149faa0abad586b4db122
Quellennotizuspto-grants-1997_04