HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 7-(4-Fluorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18472577 | HCID 18472577 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-(4-Fluorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylic acid | HCID 18472287 | 86% |
Reaction Steps
To methyl 7-(4-fluorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate (0.27 g) were added THF (5.0 ml), ethanol (10.0 ml) and 2N sodium hydroxide solution (1.0 ml), and the mixture was stirred at room temperature for 19 hours. Under reduced pressure, the solvent was removed, and the residue was diluted with water (100 ml). The aqueous layer was made acidic with hydrochloric acid, and the mixture was extracted with ethyl acetate (100 ml). The organic layer was dried with anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was crystallized and washed with hexane to give 7-(4-fluorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylic acid (0.22 g, 86%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06413947B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-b32fa6c518a5475191a50fdaebcecd5f |
| Source note | uspto-grants-2002_07 |