HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyltributylstannane → 5-(2-Propen-1-yl)quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyltributylstannane | HCID 90628 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 5-Bromoquinoline | HCID 817321 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(2-Propen-1-yl)quinoline | HCID 22504110 | 95.9% |
Reaction Steps
5-Bromo-quinoline (5.6 g, 27 mmol) was dissolved in 40 mL toluene. BHT (50 mg) was added, along with allyl tributyl stannane (9.3 mL, 30 mmol), and tetrakis(triphenyl)phospine palladium (600 mg, 0.52 mmol). The reaction was refluxed overnight, then cooled. Potassium fluoride solution (1.0 g, in 18 mL H2O) was added. The reaction was stirred for 3 hours, then filtered. The reaction mixture was concentrated in vacuo. It was chromatographed in 3:1 hexane/ethyl acetate to yield 4.38 g (95%) of 5-allyl-quinoline as a yellow oil. MS (APCI) m/z 170.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06875765B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-57d2c7034a9c4c66b186e7b5d0fbf3e6 |
| Source note | uspto-grants-2005_04 |