HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 67024288, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178515651 | HCID 178515651 | — |
| Solvent | Chloromethyl Methyl Ether | HCID 7864 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 67024288 | HCID 67024288 | — |
Reaction Steps
To a solution of 5-(4-(benzyloxy)phenyl)isoxazol-3-ol (1.38 g) in tetrahydrofuran (30 ml), 2.15 ml of triethylamine and 0.51 ml of methoxymethyl chloride were added, and the reaction solution was stirred overnight at room temperature. A saturated aqueous ammonium chloride solution was added to the reaction solution, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with a saturated saline solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified by silica gel column chromatography (eluent: ethyl acetate/hexane (10:90-0:100)) to afford the title compound as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367708B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-5837cd8ae23f41ab95e191c9ef37f3f2 |
| Source note | uspto-grants-2013_02 |