Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 7-Chloro-4-(furan-3-yl)quinoline | HCID 23370170 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Catalyst | HCID 178418745 | HCID 178418745 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(Furan-3-yl)-7-methylquinoline | HCID 23370177 | — |
Reaction Steps
To a mixture of 7-chloro-4-(furan-3-yl)quinoline (30.2 g) and [1,3-bis(diphenylphosphino)propane]nickel (II) chloride (7.1 g) in Et2O (950 mL) was added MeMgBr (141 mL, 1.4M in 3:1 THF:toluene) at such a rate to maintain a temperature of 30° C. The mixture was refluxed for 30 min., cooled to 0° C. and saturated NH4Cl (200 mL) was added followed by H2O (100 mL). The layers were separated and the aqueous phase was extracted with EtOAc. The combined organics were washed with NH4OAc buffer, brine, dried (MgSO4) and concentrated. Chromatography (silica gel;EtOAc/hexane (3:7)) provided the title compound as a beige oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05552437 |
|---|
| Source dataset | uspto-grants-1996_09 |
|---|
| ORD ID | ord-07cefc43d8834002ad853d126d18dce2 |
|---|
| Source note | uspto-grants-1996_09 |
|---|