Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | 4-Methylpyridine | HCID 7963 | — |
| Product | HCID 53851086 | HCID 53851086 | 83% |
Reaction Steps
220 g of 4-methylpyridine and 1.0 g of solid base G were fed into a 1000 ml autoclave equipped with an electromagnetic stirrer under an atmosphere of nitrogen, and then heated to 140° C. with stirring at 700 r.p.m. Subsequently, 16.5 g of butadiene was added to the mixture in 1 hour. After the reaction, the autoclave was cooled and the catalyst was removed by filtration. The reaction solution was analyzed by gas chromatography. 4-(3-pentenyl)pyridine was obtained in a 83% yield based on 4-methypyridine consumed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06008364 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-96d79fb38a72475db7a0bb033a236b22 |
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| Source note | uspto-grants-1999_12 |
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