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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 532541Erstellt: 23. Oktober 2026

Hydrochloric Acid → 5-Benzoyl-5,6-dihydro-cyclopenta[b]thiophen-4-one

https://huagongshe.com/de/reaction/532541

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPhenyl benzoateHCID 7169—
EduktSodium hydrideHCID 24758—
Edukt4H,5H,6H-cyclopenta[b]thiophen-4-oneHCID 1958632—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-Benzoyl-5,6-dihydro-cyclopenta[b]thiophen-4-oneHCID 8669919873%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

5,6-Dihydro-cyclopenta[b]thiophen-4-one (3.34 g, 24.2 mmol) in 40 mL of THF was treated with NaH (60 percent, 1.45 g, 36.25 mmol). After the addition of Benzoic acid phenyl ester, the reaction mixture was heated at 100° C. for 8 hr. The solution was cooled to room temperature and poured into water. The resulting mixture was acidified with concentrated HCl and was added with ethyl acetate (80 mL). The organic layer was collected, brined, dried over MgSO4(s), and concentrated under reduced pressure. The resultant precipitate was collected and recrystallized from ethanol to provide the corresponding 5-Benzoyl-5,6-dihydro-cyclopenta[b]thiophen-4-one (4.3 g, 17.7 mmol) as white solid in 73% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08853207B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-3106beaad0234cb4964de82aa2c0dbef
Quellennotizuspto-grants-2014_10