HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 4-(allyloxy)-3-bromobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-4-hydroxybenzaldehyde | HCID 76308 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(allyloxy)-3-bromobenzaldehyde | HCID 2716613 | — |
Reaction Steps
3-Bromo-4-hydroxybenzaldehyde (20.1 g, 0.100 mol) and allyl bromide (14.5 g, 0.120 mol) were heated under reflux together with potassium carbonate (20.7 g, 0.150 mol) in 150 ml acetone (abs.) for 8 hours. After cooling, the solid was filtered off and washed with acetone. After complete concentration of the organic phase, there was obtained an oily residue that was used directly in the second step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07393367B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-495f487bedfe4f41ae76334d5dcc0546 |
| Source note | uspto-grants-2008_07 |