HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-Benzyloxy-3-ethyl-5-methylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Ethyl-4-hydroxy-5-methylbenzaldehyde | HCID 23159210 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Benzyloxy-3-ethyl-5-methylbenzaldehyde | HCID 86639348 | 73.2% |
Reaction Steps
To a solution of 3-ethyl-4-hydroxy-5-methyl-benzaldehyde (8.00 g, 48.7 mmol) in acetone (130 mL), K2CO3 (20.2 g, 146.2 mmol) followed by benzylbromide (12.5 g, 73.1 mmol) is added. The suspension is stirred at reflux for 16 h before it is filtered and the solvent of the filtrate is removed in vacuo. The residue is separated by CC on silica gel to give 4-benzyloxy-3-ethyl-5-methyl-benzaldehyde (9.07 g) as a pale yellow oil; LC-MS: tR=1.09 min, [M+1]+=255.08.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044076B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-9227861861ea4721af7554b752c562fa |
| Source note | uspto-grants-2011_10 |