HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-(Benzyloxy)-3-methylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxy-3-methylbenzaldehyde | HCID 139901 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(Benzyloxy)-3-methylbenzaldehyde | HCID 20298646 | — |
Reaction Steps
A mixture of 4-hydroxy-3-methylbenzaldehyde (0.658 g), benzyl bromide (0.812 g) and potassium carbonate (1.0 g) in acetone (30 ml) was stirred and heated under reflux for 6 hours. The solvent was removed and the residues were partitioned between water and ethyl acetate. The aqueous phase was further extracted with ethyl acetate and the combined organic layers were washed with brine and dried. Removal of the solvent gave the title compound as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07196107B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-c8e9719a888c432a9cdd092fbd39e4ec |
| Source note | uspto-grants-2007_03 |