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 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(Benzhydryloxy)-2-nitrobenzene | HCID 7434122 | — |
Reaction Steps
2-Nitrophenol (11.0 g, 79 mmole), anhydrous potassium carbonate (17.6 g, 127.4 mmole) and benzhydryl bromide (19.6 g, 79 mmol) in acetone (220 ml) were refluxed under nitrogen for 5 hours. The mixture was cooled, filtered and evaporated in vacuo. The residue was triturated with diethyl ether, filtered and evaporated. Trituration with 60°-80° C. petroleum ether yielded a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05281593 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-bf579edc0ce849fe8869e66392514941 |
| Source note | uspto-grants-1994_01 |