Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1864611Erstellt: 26. Oktober 2026

Oxalyl chloride → 6-Methoxy-1-benzothiophene-2,3-dione

https://huagongshe.com/reaction/1864611

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxalyl chlorideHCID 65578—
Edukt3-MethoxybenzenethiolHCID 84989—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelDiethyl EtherHCID 3283—
Produkt6-Methoxy-1-benzothiophene-2,3-dioneHCID 344084847%

Reaktionsschritte

To a solution of 3-methoxythiophenol (26.7 mmol) in ether (20 mL) was added oxalyl chloride (43 mmol) dropwise. The mixture was heated at reflux for 1.5 h, cooled to rt, and concentrated in vacuo. The resulting yellow oil was dissolved in dichloromethane (50 mL), cooled to 0° C., and was treated with aluminum chloride (32.0 mmol) in portions. The mixture was heated at reflux for 30 min, cooled to rt, and poured onto ice water with stirring. The organic layer was separated and successively washed with saturated, aqueous sodium bicarbonate, water, and brine. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography (4/1 ethyl acetate/hexane) which provided 6-methoxy-1-benzothiophene-2,3-dione (47%) as an orange solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07625924B2
Quelldatensatzuspto-grants-2009_12
ORD IDord-d28adc8a888f4d9b8bea1d56c6e9dc3a
Quellennotizuspto-grants-2009_12