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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508958Generated: November 2, 2026

2-(Tributylstannyl)furan → HCID 90338574, compound

https://huagongshe.com/reaction/1508958

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
Reactant2,4-Dichloro-6,7-dihydro-5H-cyclopenta[b]pyridineHCID 12214817—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 90338574HCID 9033857492.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 2,4-dichloro-6,7-dihydro-5H-cyclopenta[b]pyridine (0.130 g, 0.69 mmol) in dioxane (3 mL) was added tributyl(furan-2-yl)stannane (0.271 g, 0.76 mmol) and tetrakis(triphenylphosphine)palladium (0.039 g, 0.035 mmol). The mixture was purged with nitrogen and then heated to 110° C. under sealed conditions for 2 h. After this time, the mixture was diluted with water and extracted with ethyl acetate. The organic layer were dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, hexanes/ethyl acetate) to afford the title compound (0.140 g, 92%) as a white solid. MW=219.67. 1H NMR (CDCl3, 500 MHz) δ 7.52-7.48 (m, 1H), 7.45 (s, 1H), 7.02-6.98 (m, 1H), 6.52-6.48 (m, 1H), 3.10 (t, J=7.5 Hz, 2H), 2.99 (t, J=7.5 Hz, 2H), 2.15 (quin, J=7.5 Hz, 2H); APCI MS m/z 220 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-ce25532bb8f647e88d3e52100e7b2719
Source noteuspto-grants-2015_12