HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85213Generated: October 29, 2026
Tri(butyl)vinyltin → HCID 59410189, compound
https://huagongshe.com/reaction/85213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tri(butyl)vinyltin | HCID 53438229 | — |
| Reactant | 3-Bromo-1-[2-(methoxymethyl)-4-nitrophenyl]pyridin-2(1H)-one | HCID 59410197 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59410189 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846934B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2711c33360944690a0e7968780759bce |
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| Source note | uspto-grants-2014_09 |
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