HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Benzaldehyde, 3-iodo-5-methoxy-4-(2-propenyloxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzaldehyde, 4-hydroxy-3-iodo-5-methoxy- | HCID 79499 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzaldehyde, 3-iodo-5-methoxy-4-(2-propenyloxy)- | HCID 4382547 | — |
Reaction Steps
Allyl bromide (27.5 ml, 0.32 mol) was added to a solution of 5-iodovanillin (50.0 g, 0.18 mol) in DMF (200 ml) containing potassium carbonate (48 g, 0.35 mol) at 80° C. The mixture was stirred at this temperature for 1 hour, filtered, and the filtrate was evaporated to a residue, which was purified by HPLC (hexane-ethyl acetate, 4:1, v/v) to give 4-allyloxy-5-iodo-3-methoxybenzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05010100 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-09b2db7817de4c739fa1efd09c4a4ec5 |
| Source note | uspto-grants-1991_04 |