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 K2CO3 (8.9 g, 64.4 mmol). The mixture is stirred at ambient temperature overnight, diluted with water and extracted with EtOAc. The organic phase is washed with aqueous K2CO3 and brine, dried over MgSO4, filtered and concentrated to afford 3-benzyloxy-4-nitrobenzaldehyde as a yellow solid: MS (M+H)+=258.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119666B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-bc8ed470fa644b76912b2e450ab1fffd |
| Source note | uspto-grants-2012_02 |