HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-Hydroxy-4-phenyl-2-propylquinoline-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 3-Oxohexanenitrile | HCID 9793723 | — |
| Reactant | (2-Amino-5-{[tert-butyl(dimethyl)silyl]oxy}-phenyl)(phenyl)methanone | HCID 68832602 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Hydroxy-4-phenyl-2-propylquinoline-3-carbonitrile | HCID 68833314 | 56% |
Reaction Steps
A solution of (2-amino-5-{[tert-butyl(dimethyl)silyl]oxy}-phenyl)(phenyl)methanone (2.0 g, 6.1 mmol), 3-oxohexanenitrile (0.81 g, 7.3 mmol) and methanesulfonic acid (0.59 g, 6.1 mmol) in toluene (50 ml) was stirred at 110° C. for 15 hrs. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was crystallized from disopropyl ether to give 6-hydroxy-4-phenyl-2-propylquinoline-3-carbonitrile (0.98 g, yield 56%) as pale-yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07547710B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-ff61c76a1bb24130b897e26ad54355ac |
| Source note | uspto-grants-2009_06 |