HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 4-(1-Oxo-indan-5-yloxy)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-(1-Oxo-indan-5-yloxy)-benzonitrile | HCID 59750643 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4-(1-Oxo-indan-5-yloxy)-benzamide | HCID 59750663 | 5.8% |
Reaction Steps
Combine 4-(1-Oxo-indan-5-yloxy)-benzonitrile (1.64 g, 6.58 mmol), tert-butyl alcohol (50 ml), and grounded KOH (1.85 g, 32.89 mmol) at room temperature under nitrogen atmosphere. Stir the reaction for 24 hours then concentrate under reduced pressure. Add Ethyl acetate to the reaction mixture and wash with brine. Dry the organic layer over Na2SO4. A yellow-mange solid precipitates out to afford 101.0 mg, 0.38 mmol (5.7% yield) of the title compound: No Characterization—Characterized by sequential reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101638B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-6f3198d2da994130a586221560d03f30 |
| Source note | uspto-grants-2012_01 |