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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85213Generated: October 29, 2026

Tri(butyl)vinyltin → HCID 59410189, compound

https://huagongshe.com/reaction/85213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri(butyl)vinyltinHCID 53438229—
Reactant3-Bromo-1-[2-(methoxymethyl)-4-nitrophenyl]pyridin-2(1H)-oneHCID 59410197—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59410189HCID 59410189—

Reaction Steps

94 g (277 mmol) of the compound from Example 28A are dissolved in 1.2 l of anhydrous dioxane, and 8 g (6.9 mmol) of tetrakis(triphenylphosphine)palladium(0) are added. At room temperature, 105 g (333 mmol) of tributylvinyltin are added slowly, and after the addition has ended, the mixture is heated at reflux for 21 h. The reaction solution is allowed to cool and filtered through kieselguhr. The filter cake is washed with ethyl acetate and the combined organic filtrates are concentrated to dryness under reduced pressure. The residue that remains is dissolved in dichloromethane and applied to kieselguhr. The product is chromatographed on 1.2 kg of silica gel using a gradient of cyclohexane and ethyl acetate. The product-containing fractions are combined and concentrated to dryness under reduced pressure. This gives 23 g (29% of theory) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846934B2
Source datasetuspto-grants-2014_09
ORD IDord-2711c33360944690a0e7968780759bce
Source noteuspto-grants-2014_09