HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → 4-[6-Benzyloxy-2-(4-fluoro-phenyl)-naphthalen-1-yloxy]-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-[6-Benzyloxy-2-(4-fluoro-phenyl) naphthalen-1-yloxy]-benzaldehyde | HCID 86626528 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[6-Benzyloxy-2-(4-fluoro-phenyl)-naphthalen-1-yloxy]-phenol | HCID 57552559 | 73% |
Reaction Steps
Add 18M H2SO4 (1 mL, 16.8 mmol) dropwise into a solution of H2O2 (1 mL, 9.7 mmol) and 4-[6-benzyloxy-2-(4-fluoro-phenyl)-naphthalen-1-yloxy]-benzaldehyde at 0° C. and stir at room temperature for 12 hours. Add H2O (20 mL) and CH2Cl2 (100 mL). Separate layers and extract the aqueous layer with CH2Cl2 (2×50 mL). Combine the organic layers, dry with magnesium sulfate and concentrate in vacuo to obtain 1.88 g (73%) of the title compound: mass spectrum (ion spray) m/z=435.1 (M−H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08217032B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-460ab5ef25d647cca91f11715829e293 |
| Source note | uspto-grants-2012_07 |