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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720574Generated: October 28, 2026

2-(Tributylstannyl)furan → HCID 21893410, compound

https://huagongshe.com/reaction/720574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)furanHCID 4393688—
ReactantN-(2-(4-Bromophenyl)propyl)propane-2-sulfonamideHCID 9927066—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 21893410HCID 2189341051%

Reaction Steps

To a solution of 0.5 g (1.6 mmol) of material from Example 27 and 0.6 g (1.7 mmol) of 2-(tributylstannyl)-furan in 5 mL of dioxane was added 0.1 g (0.1 mmol) of tetrakis(triphenylphosphine)palladium (0). The mixture was heated to reflux for 16 hours, cooled to ambient temperature and diluted with 5 mL of ethyl ether. The mixture was washed once with 5 mL of saturated aqueous potassium fluoride, the organic layer was separated and the aqueous portion was extracted three times with 5 mL each of ethyl ether. The combined organics were dried (MgSO4), filtered and concentrated in vacuo. Chromatography (25 g of silica gel, 25% ethyl acetate/hexane) of the residue afforded a yellow oil which was recrystallized from ethyl ether/hexane to afford 0.2 g (51%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135487B2
Source datasetuspto-grants-2006_11
ORD IDord-3cdbf40ed94140ba99601b8d0b832e89
Source noteuspto-grants-2006_11