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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22361Erstellt: 23. Oktober 2026

Potassium Iodide → 6-(cyclopentyloxy)-7-hydroxy-2H-1-benzopyran-2-one

https://huagongshe.com/de/reaction/22361

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktBromocyclopentaneHCID 8728—
EduktPotassium CarbonateHCID 11430—
Edukt7-(benzyloxy)-6-hydroxy-2H-chromen-2-oneHCID 1204535—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-(cyclopentyloxy)-7-hydroxy-2H-1-benzopyran-2-oneHCID 19927742—

Reaktionsschritte

50.0 g (186 mmol) of 6-hydroxy-7-phenylmethoxy-2H-1-benzopyran-2-one, 41.7 g (280 mmol) of cyclopentylbromide, 51.4 g (372 mmol) of potassium carbonate and 5.0 g of potassium iodide are agitated in 500 ml DMF for 18 h at 80° C. This is followed by filtration, evaporation, dissolution in chloroform, washing with water, drying over sodium sulfate and renewed evaporation: yield: 60.0 g (96%) of 6-(cyclopentyloxy)-7-(phenylmethoxy)-2H-1-benzopyran-2-one, fusion point 140°-141° C. (from isopropanol). Of this 15.0 g (45 mmol) in 200 ml ethanol are hydrogenated in the presence of 2.0 g Pd on active carbon (5%) for 3 h at 25° C. and 7 bar hydrogen pressure. After filtration the solvent is removed: yield 9.0 g (82%), fusion point 154°-155° C. (from isopropanol and TBME).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428038
Quelldatensatzuspto-grants-1995_06
ORD IDord-fdec0f046a2d4bc29dd9bda843e2c9dd
Quellennotizuspto-grants-1995_06