HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → 5-Bromobenzo[c]phenanthrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-4-[2-(2-methoxyvinyl)phenyl]naphthalene | HCID 67607495 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromobenzo[c]phenanthrene | HCID 10662482 | 15% |
Reaction Steps
180 g of 1-bromo-4-[2-(2-methoxyvinyl)phenyl]naphthalene and 1.0 L of dichloromethane were placed. 25 mL of methanesulfonic acid was added at room temperature while stirring. The stirring was conducted for 8 hours at room temperature. After the completion of the reaction, 1 L of an aqueous solution of 10% potassium carbonate was added. After removing an aqueous phase, an organic phase was washed with water and saturated saline, and dried with magnesium sulfate. After filtering off magnesium sulfate, the organic phase was concentrated. The residues were purified by silica gel column chromatography, whereby 24.4 g (yield 15%) of 5-bromobenzo[c]phenanthrene as an intended product was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126943B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-408cf63e92c54a2284cfc0b9890a1ff1 |
| Source note | uspto-grants-2015_09 |