HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 3-Iodo-4,5-dimethoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Iodovanillin | HCID 53732425 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Iodo-4,5-dimethoxybenzaldehyde | HCID 2778113 | 90.5% |
Reaction Steps
To a stirred, cooled (0° C.) solution of iodovanillin (10.0 g, 35.96 mmol.) in dimethylformamide (50 mL) was added anhydrous potassium carbonate (20.0 g, 143.86 mmol.) followed by iodomethane (3.11 mL, 50.0 mmol.). The mixture was allowed to warm to ambient temperature and stir for 14 H. The mixture was poured into diethyl ether (500 mL) and washed with water (3×150 mL). The organic phase was dried over MgSO4 and concentrated under reduced pressure to afford 3-iodo-4,5-dimethoxybenzaldehyde (9.5 g) as a yellow oil which solidified upon standing and was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705519 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-6114b4bdf5514a1f85deb23a75e7bbc3 |
| Source note | uspto-grants-1998_01 |