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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532541Generated: October 26, 2026

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

https://huagongshe.com/reaction/532541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenyl benzoateHCID 7169—
ReactantSodium hydrideHCID 24758—
Reactant4H,5H,6H-cyclopenta[b]thiophen-4-oneHCID 1958632—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-Benzoyl-5,6-dihydro-cyclopenta[b]thiophen-4-oneHCID 8669919873%

Reaction Conditions

Temperature100 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853207B2
Source datasetuspto-grants-2014_10
ORD IDord-3106beaad0234cb4964de82aa2c0dbef
Source noteuspto-grants-2014_10