Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-Bromoindole | HCID 24905 | — |
| Reactant | 3-Formylphenylboronic acid | HCID 2734356 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(1H-indol-5-yl)benzaldehyde | HCID 4135879 | 57% |
Reaction Steps
A mixture of 5-bromo-indole (8.7 g, 44.4 mmol), 3-formylbenzeneboronic acid (10 g, 66.7 mmol), cesium carbonate in water (2M, 88.8 mL, 178 mmol) in 450 mL of dioxane was degassed (evacuate in vacuo and pressurize with nitrogen, 3 times) PdCl2(dppf).DCM (1.1 g, 1.3 mmol) was added and the mixture degassed one more time as described above. The resulting mixture was heated at 100° C. for 3 h, then it was allowed to cool to room temperature and partitioned between diethyl ether and water. The aqueous phase was extracted with diethyl ether and the combined organic phases were washed with water, brine, dried over MgSO4, filtered and evaporated to give the crude product. Chromatography on silica gel (elution with ethyl acetate/heptane) afforded 5.6 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07625889B2 |
|---|
| Source dataset | uspto-grants-2009_12 |
|---|
| ORD ID | ord-168053c28ba84e3c8056cba3d19a2d6c |
|---|
| Source note | uspto-grants-2009_12 |
|---|