HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 4-Fluoro-3-methylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 5-Bromo-2-fluorotoluene | HCID 123527 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Fluoro-3-methylbenzaldehyde | HCID 2734874 | — |
Reaction Steps
A solution of 5-bromo-2-fluorotoluene (6 g) in ethyl ether (10 ml) and a catalytic amount of iodine were added to a suspension of magnesium (960 mg) in ethyl ether (10 ml) under nitrogen atmosphere and the whole was refluxed for 30 minutes. After cooling, a solution of ethyl orthoformate (5.4 g) in ethyl ether (20 ml) was added to the mixture and the whole was stirred overnight. Sulfuric acid (10%, 20 ml) was added to the mixture and the organic layer was separated, washed with brine, dried over sodium sulfate, and evaporated. The residue was purified by column chromatography on silica gel with a mixture of hexane and ethyl acetate (10:1) as eluent to give 4-fluoro-3-methylbenzaldehyde as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166598B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-98632e66786e46c59a1afab21c3c510e |
| Source note | uspto-grants-2007_01 |