HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 2-Fluoro-6-iodobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Fluoro-6-iodobenzonitrile | HCID 522722 | — |
| Reactant | Diisobutylaluminumhydride toluene | HCID 86583787 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Fluoro-6-iodobenzaldehyde | HCID 11096976 | 83% |
Reaction Steps
2-Fluoro-6-iodobenzonitrile (10.274 g) was dissolved in Toluene (100 ml), followed by the dropwise addition of 1.5M diisobutylaluminum hydride/toluene solution (31 ml) in nitrogen atmosphere at −70° C., and the mixture was stirred for 25 min. Subsequently, it was stirred at room temperature for further 45 min. To the mixture was added 5% sulfuric acid and it was stirred for 1 hr. Sequentially, the resulting solution was extracted with ethyl acetate, and the resulting organic layer was washed with water, dried (over MgSO4) and evaporated. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane system), to give the title compound as yellow oil (8.683 g, yield; 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06875761B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-a87786f4ad974a34a6a98367745e7b42 |
| Source note | uspto-grants-2005_04 |