HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481374Generated: October 31, 2026
HCID 20597910, compound → HCID 12201445, compound
https://huagongshe.com/reaction/1481374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20597910 | HCID 20597910 | — |
| Reactant | Tri(butyl)vinyltin | HCID 53438229 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | HCID 12201445 | HCID 12201445 | 41% |
Reaction Steps
The title compound was prepared by following general procedure 2. 5-Bromo-2-propyl-pyridine (0.5 g, 2.5 mmol) was dissolved in DMF:THF (3:1, 8 mL). To this solution, tributylvinyltin (1.3 mL, 3.7 mmol) and Pd(PPh3)4 (0.057 g, 0.05 mmol) was added at RT under nitrogen and was heated at 100° C. for 2 h. The reaction mixture was cooled to RT and diluted with water (80 mL) and extracted with DCM (3×100 mL), the organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure using rotary evaporator below 40° C. The crude was purified through column chromatography (3% ethylacetate:hexane in silica 100-200 mesh, Diameter of column—2.5.0 cm, Height of silica—approx. 5 inch) to provide 2-propyl-5-vinylpyridine as a light yellow liquid (0.15 g, 41% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409910B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-ab455b62381e4c3fa4b0a9786cb7ae88 |
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| Source note | uspto-grants-2016_08 |
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