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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1169467Erstellt: 26. Oktober 2026

Hydrochloric Acid → 7-(4-Propoxyphenoxy)-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylic acid

https://huagongshe.com/reaction/1169467

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
EduktMethyl 7-(4-propoxyphenoxy)-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylateHCID 22989987—
LösungsmittelMeOH tetrahydrofuranHCID 21899815—
Produkt7-(4-Propoxyphenoxy)-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylic acidHCID 2299017575,5%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

Into a solution of methyl 7-(4-propoxyphenoxy)-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylate (0.31 g) in THF-methanol (5-2.5 ml) was added at room temperature a 1 M aqueous solution of potassium carbonate (1.5 ml), and the resulting mixture was stirred at 65° C. for 40 hours. After cooling to room temperature, 1 N hydrochloric acid (10 ml) was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated solution of sodium chloride and was dried with magnesium sulfate. After concentration under reduced pressure, the precipitated crystals were collected by filtration. The crystals were washed with diisopropyl ether to obtain 7-(4-propoxyphenoxy)-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylic acid (226 mg) as light yellow crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06627651B1
Quelldatensatzuspto-grants-2003_09
ORD IDord-e24de21db28e466abdd87324a3d1d590
Quellennotizuspto-grants-2003_09