HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391748Generated: October 29, 2026
Tri(butyl)vinyltin → HCID 59410169, compound
https://huagongshe.com/reaction/391748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tri(butyl)vinyltin | HCID 53438229 | — |
| Reactant | 3-Bromo-1-(2,6-dimethyl-4-nitrophenyl)pyridin-2(1H)-one | HCID 59410207 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59410169 | HCID 59410169 | — |
Reaction Steps
132 g (408 mmol) of the compound from Example 59A (alternative synthesis) are dissolved in 1.27 l of anhydrous dioxane, 136 g (428 mmol) of tributylvinyltin and 9.44 g (8.17 mmol) of tetrakis(triphenylphosphine)palladium are added and the mixture is stirred at 100° C. for 4 h. The mixture is allowed to cool and filtered through kieselguhr. The mixture is concentrated to dryness under reduced pressure. The residue is dissolved in dichloromethane and purified by chromatography on silica gel (petroleum ether/ethyl acetate 9:1, then 8:2, then 7:3). The product-containing fractions are combined, the solvents are removed and the residue is triturated with petroleum ether/diethyl ether (10:1). This gives 83 g (75% of theory) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383822B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-1a4f64756ffe4630ad0d0bb2413bd9f2 |
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| Source note | uspto-grants-2013_02 |
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