HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Tributylstannyl)furan → HCID 15429322, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Tributylstannyl)furan | HCID 4393688 | — |
| Reactant | HCID 15429321 | HCID 15429321 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15429322 | HCID 15429322 | 105.9% |
Reaction Steps
A suspension of 1.32 g (5.0 mmol) of 7-bromo-1,2,3,5-tetrahydrocyclo-penta[c]quinolin-4-one in 200 mL of toluene is mixed with 1.7 ml (5.5 mmol) of 2-(tributyl-stannyl)furan and 0.29 g (0.25 mmol) of tetrakis(triphenylphosphine)palladium. The reaction mixture is degassed, aerated with nitrogen, stirred for 15 hours at room temperature and heated for 4.5 hours to 110° C. The batch is mixed with silica gel and concentrated by evaporation in a vacuum. Column chromatography of the residue on silica gel with hexane-ethyl acetate yields 1.33 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067667B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-0edcfa47a2bc45af8150c536366d52de |
| Source note | uspto-grants-2006_06 |