HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromoisoquinoline → HCID 10942859, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromoisoquinoline | HCID 73743 | — |
| Reactant | Allyltributylstannane | HCID 90628 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10942859 | HCID 10942859 | — |
Reaction Steps
To a solution of 4-bromoisoquinoline (2.0 g) in 70 mL of toluene was added allyl tributyl stannane (3.28 mL) and Pd(PPh3)4 (1.10 g). The resulting solution was heated at reflux for 12 hours and then cooled to room temperature. The solution was concentrated in vacuo, dissolved in ether and washed successively with an aqueous solution of trithiocyanuric acid trisodium salt, water and brine. The organic layer was then dried over magnesium sulfate, filtered, concentrated in vacuo, and purified using flash chromatography (silica, 0-30% EtOAc/hexanes) to provide 0.965 g of 4-(2-propenyl)-isoquinoline. Mass spectrum [NH3/CI], (M+H)+=170.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06331545B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-1620ac7e059c43468bb092b65bb0e578 |
| Source note | uspto-grants-2001_12 |