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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897379Generated: October 31, 2026

4-tributylstannyl-5H-furan-2-one → HCID 22346469, compound

https://huagongshe.com/reaction/897379

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tributylstannyl-5H-furan-2-oneHCID 10915702—
ReactantHCID 22346452HCID 22346452—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
ProductHCID 22346469HCID 22346469—

Reaction Steps

The iodide from step 2 (4.37 g, 10.32 mmol) was dissolved in anhydrous toluene (40 ml) in an oven dried flask that was purged with nitrogen. Dichlorobis(triphenylphospine)palladium (II) (660 mgs., 0.94 mmol) and 4-(tributylstannyl)furan-2(5H)-one, (3.85 g, 10.32 mmol) (prepared as described by Gregory J. Hollingworth, Gemma Perkins, and Joseph Sweeney, J. Chem. Soc., Perkins 1. 1996, 1913) were then added to the reaction. After four hours at reflux the reaction was cooled and the solids that precipitated from the solution were collected by vacuum filtration. The product contained 17% of an impurity: N,N′-bis(4-fluorobenzyl)-8,8′-dihydroxy-5,5′-bi-1,6-naphthyridine-7,7′-dicarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921759B2
Source datasetuspto-grants-2005_07
ORD IDord-4fc55660dccf4039862341bf69191dfa
Source noteuspto-grants-2005_07