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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121725Generated: November 3, 2026

1,3-Dichloro-5,6-dihydro-4H-cyclopenta(c)thiophen-4-one → HCID 23434091, compound

https://huagongshe.com/reaction/2121725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dichloro-5,6-dihydro-4H-cyclopenta(c)thiophen-4-oneHCID 315616—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Fluorophenylboronic acidHCID 2734354—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 23434091HCID 2343409137%

Reaction Steps

To a stirred solution of 1,3-dichloro-5,6-dihydro-4H-cyclopenta(c)thiophene-4-one (250 mg, 1.21 mmol) in DME (7.5 mL) was added 2-fluorobenzeneboronic acid (177 mg, 1.27 mmol), saturated aqueous NaHCO3 solution (2.5 mL) and bis(triphenylphosphine)palladium(II)chloride (100 mg, 0.14 mmol) at room temperature under nitrogen. The mixture was heated at reflux temperature for 8 hours. The whole was extracted with ethyl acetate (50 mL×2), and the combined organic layers were washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with hexane-ethyl acetate (10:1) to provide the subtitle compound (118 mg, 37% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696470B2
Source datasetuspto-grants-2004_02
ORD IDord-ad9aa953aef341b1a1fcc95a6d04acd2
Source noteuspto-grants-2004_02