HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 4-(Allyloxy)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 11768857 | HCID 11768857 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(Allyloxy)benzaldehyde | HCID 95942 | — |
Reaction Steps
4-allyloxybenzaldehyde was prepared by reaction of allyl bromide on 4-hydroxybenzaldehyde in refluxing acetone in the presence of K2CO3. The distilled product was used as a precursor for 4-allyloxystyrene synthesis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05084490 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-633ea9a940cf4712b2f2df2f415d2e86 |
| Source note | uspto-grants-1992_01 |