HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 6-Methoxy-7-methyl-1-phenoxyisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Chloro-6-methoxy-7-methylisoquinoline | HCID 53782880 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 6-Methoxy-7-methyl-1-phenoxyisoquinoline | HCID 66941784 | 19.6% |
Reaction Steps
A mixture of 1-chloro-6-methoxy-7-methyl-isoquinoline (9 g, 43.48 mol), phenol (16.3 g), potassium hydroxide (9.45 g) and xylene (100 ml) was refluxed for 4 days. The reaction mixture was poured out into aqueous sodium hydroxide (4 M) and the xylene layer separated. The aqueous layer was extracted twice with toluene. The combined organic layers were dried (Na2SO4) and concentrated in vacuo to give a residue. The residue was purified by flash chromatography using dichloromethane gave 6-methoxy-7-methyl-1-phenoxyisoquinoline (9 g, 33.96 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893088B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-f69c57d012bd4562b8f92e58c39a4652 |
| Source note | uspto-grants-2011_02 |