HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279446Generated: October 30, 2026
Sulfuric Acid → 2-(2,5-Dimethylphenoxymethyl)phenyl isoxazol-3-yl ketone
https://huagongshe.com/reaction/279446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Bromobenzyl-(2,5-dimethylphenyl)ether | HCID 10946216 | — |
| Reactant | 1,2-Oxazole-3-carbonitrile | HCID 22624610 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2,5-Dimethylphenoxymethyl)phenyl isoxazol-3-yl ketone | HCID 10902875 | 6.3% |
Reaction Steps
THF (2 ml) and bromoethane (0.1 ml) were added to magnesium (0.49 g, 0.02 mol) in a stream of nitrogen, and the mixture was stirred at 50° C. for 10 minutes. Then, a mixture of 1-bromo-2-(2,5-dimethylphenoxymethyl)benzene (2.91 g, 0.01 mol) and THF (8 ml) was added at 50 to 60° C. over 30 minutes, and the mixture was stirred at 50 to 60° C. for 1 hour. After completion of the reaction, the reaction mixture was added to a mixture of 3-cyanoisoxazole (1.45 g, 0.015 mol) and THF (15 ml) at 20° C. or lower over 15 minutes, and then the mixture was stirred at room temperature for 2 hours. After completion of the reaction, 2N sulfuric acid (200 ml) was added, and the mixture was extracted with ether. The ether layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate/n-hexane) and recrystallized from n-hexane to give 2-(2,5-dimethylphenoxymethyl)phenyl isoxazol-3-yl ketone (0.20 g, 6.3%) as colorless crystals. mp. 90.5-92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06362212B1 |
|---|
| Source dataset | uspto-grants-2002_03 |
|---|
| ORD ID | ord-4aeffda511844029a092d2c64a9a3057 |
|---|
| Source note | uspto-grants-2002_03 |
|---|