HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508958Generated: November 2, 2026
2-(Tributylstannyl)furan → HCID 90338574, compound
https://huagongshe.com/reaction/1508958
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| Reactant | 2,4-Dichloro-6,7-dihydro-5H-cyclopenta[b]pyridine | HCID 12214817 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 90338574 | HCID 90338574 | 92.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221843B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-ce25532bb8f647e88d3e52100e7b2719 |
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| Source note | uspto-grants-2015_12 |
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