HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 23034795, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Difluoromethoxy)-3-hydroxybenzaldehyde | HCID 2758295 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 23034795 | HCID 23034795 | — |
Reaction Steps
A 9 g quantity of 4-difluoromethoxy-3-hydroxy benzaldehyde was dissolved in 180 ml of acetonitrile, and 13.1 g of potassium carbonate and 8.6 ml of benzyl bromide were added. The mixture was stirred at room temperature for 4 hours. After insolubles were removed by filtration, the filtrate was concentrated and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to give 11.9 g of colorless oily 3-benzyloxy-4-difluoromethoxybenzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637559B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-5bd83c7c1ddb4d748700071ba52b6a08 |
| Source note | uspto-grants-2014_01 |