HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyltriphenylphosphonium chloride → HCID 67317831, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyltriphenylphosphonium chloride | HCID 9879809 | — |
| Reactant | HCID 67317464 | HCID 67317464 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67317831 | HCID 67317831 | — |
Reaction Steps
To a mixture of methyltriphenylphosphonium chloride (0.54 g, 1.7 mmol) in THF (10 mL) at −78° C. was added n-butyllithium, 2.5 M in hexanes (0.80 ml, 2.0 mmol). After 20 min, a mixture of (7-methoxyquinolin-4-yl)(4-nitrophenyl)methanone (0.177 g, 0.57 mmol) in THF (5 mL) was slowly added. After 10 min, the mixture was allowed to warm to RT. The reaction was quenched with saturated aqueous NH4Cl. The mixture was diluted with EtOAc and washed with water and brine. After drying the organic fraction with Na2SO4, the solvent was removed in vacuo and the residue purified by silica gel chromatography using 40-100% hexanes:EtOAc to afford 7-methoxy-4-(1-(4-nitrophenyl)vinyl)quinoline as a yellow foam. MS: M+H+=307.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776857B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-d0965bc58905439e8deabee0ce4a2517 |
| Source note | uspto-grants-2010_08 |