HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Nitrophenol → 1-(Benzhydryloxy)-2-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Nitrophenol | HCID 6947 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromodiphenylmethane | HCID 236603 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(Benzhydryloxy)-2-nitrobenzene | HCID 7434122 | 39.5% |
Reaction Steps
A mixture of o-nitrophenol (2.08 g, 15.0 mmol), 1-[bromo(phenyl)methyl]benzene (3.70 g, 15.0 mmol) and potassium carbonated (K2CO3) (4.14 g, 30.0 mmol) in acetone (60 mL) was kept at reflux temperature for 5 h. The reaction mixture was cooled to room temperature, concentrated in vacuo. The residue was partitioned between dichloromethane (CH2Cl2) and water (H2O), organic layer dried over sodium sulphate (Na2SO4), filtered, concentrated. The residue was purified by silica gel flash chromatography to give subtitled compound (1.81 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07388020B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-079031298525448db5b6e52e03b4a7e2 |
| Source note | uspto-grants-2008_06 |