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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452242Generated: October 27, 2026

Tri(butyl)vinyltin → HCID 59410169, compound

https://huagongshe.com/reaction/452242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri(butyl)vinyltinHCID 53438229—
Reactant3-Bromo-1-(2,6-dimethyl-4-nitrophenyl)pyridin-2(1H)-oneHCID 59410207—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59410169HCID 59410169—

Reaction Conditions

Temperature100 °C

Reaction Steps

2.00 g (6.19 mmol) of the compound from Example 51A are dissolved in 31 ml of anhydrous dioxane, and 2.36 g (7.42 mmol) of tributylvinyltin and 143 mg (0.124 mmol) of tetrakis(triphenylphosphine)palladium are added and the mixture is stirred at 100° C. for 5 h. The mixture is allowed to cool and filtered through kieselguhr. The filter cake is washed three times with ethyl acetate, and the combined filtrates are concentrated to dryness under reduced pressure. The residue is purified by chromatography on silica gel (cyclohexane/ethyl acetate 4:1). This gives 846 mg (51% of theory) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487111B2
Source datasetuspto-grants-2013_07
ORD IDord-4d5f354978f142a2a818839414b468c7
Source noteuspto-grants-2013_07