HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 3-(Benzyloxy)-4-nitrobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Hydroxy-4-nitrobenzaldehyde | HCID 69712 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(Benzyloxy)-4-nitrobenzaldehyde | HCID 12111719 | — |
Reaction Steps
To a stirred solution of benzyl bromide (6.9 g, 40.3 mmol) and 3-hydroxy-4-nitrobenzaldehyde (9.7 g, 58.0 mmol) is added potassium carbonate (8.9 g, 64.4 mmol). The mixture is stirred at RT for 18 h, diluted with water and extracted with EtOAc. The organic phase is washed with aqueous potassium carbonate and brine, dried over MgSO4, filtered and concentrated to afford the title compound as a yellow solid: (M+1)+=258.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08084448B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-265a3e5aca85443aa0f1480bbc71275d |
| Source note | uspto-grants-2011_12 |