HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-(Benzyloxy)-3,5-difluorobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3,5-Difluoro-4-hydroxybenzaldehyde | HCID 10192584 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(Benzyloxy)-3,5-difluorobenzaldehyde | HCID 15714026 | 92% |
Reaction Steps
3,5-Difluoro-4-hydroxy-benzaldehyde obtained in Step A was dissolved in CH3CN (15 mL), and Cs2CO3(6.3 g, 19.23 mmol) was added to the solution. The mixture was cooled to 0˜5° C. Benzylbromide (1.1 mL, 9.23 mmol) was added slowly thereto, and the mixture was stirred at room temperature for 2 hours. After the termination of the reaction, the reactant was filtered and then concentrated under reduced pressure. The residue was purified by column chromatography (eluent, EtOAc/Hex=1/7) to obtain the title compound (1.76 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447044B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-a43a6fb9e8be42e3a3e74def7ffb4128 |
| Source note | uspto-grants-2016_09 |