HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → HCID 22396996, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 22396998 | HCID 22396998 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 22396996 | HCID 22396996 | 10.6% |
Reaction Steps
A mixture of 3-benzoyl-9-bromo-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (1.00 g, 2.71 mmol), phenol (0.51 g, 5.42 mmol), copper (I) oxide (0.019 g, 0.14 mmol), and cesium carbonate (2.65 g, 8.12 mmol) in o-xylene was refluxed for 24 h. After cooling to room temperature, the mixture was filtered and washed with ethyl acetate. The filtrate was concentrated in vacuo to dryness, and the residue was subjected to column chromatography (silica gel, 60% EtOAc/hexane) to afford 0.11 g (10%) of a colorless solid as the title compound: 1H NMR (300 MHz, CDCl3) δ 7.42, 7.29-7.19, 7.03-6.86, 4.12-3.91, 3.72-3.61, 3.20-3.04, 2.90-2.76; MS (ESI+) m/z 383 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06583135B2 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-b3f5423f1525432daa965412cf7dce3f |
| Source note | uspto-grants-2003_06 |