HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 22048465, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 12016671 | HCID 12016671 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 22048465 | HCID 22048465 | 86% |
Reaction Steps
A mixture of intermediate 4 (0.045 mol), iodomethane (0.225 mol) and benzyltriethylammonium chloride (0.0045 mol) in NaOH (150 ml) and THF (150 ml) was stirred overnight. EtOAc was added. The mixture was washed with water. The organic layer was separated, dried (MgSO4), filtered, and the solvent was evaporated till dryness. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/EtOAc; 95/5; 20–45 μm). The pure fractions were collected and the solvent was evaporated, yielding 13.5 g (86%) of 6-bromo-4-(3-chlorophenyl)-1-methyl-2(1H)-quinolinone (intermediate 28), melting point 182° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067531B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-95ba0882b15f42abbeb04d66d1e13868 |
| Source note | uspto-grants-2006_06 |