HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Trifluoromethoxy phenyl-N-hydroxy-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(Trifluoromethoxy)benzonitrile | HCID 67621 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Product | Trifluoromethoxy phenyl-N-hydroxy-benzamide | HCID 86643274 | — |
Reaction Steps
To a solution of 4-Trifluoromethoxybenzonitrile (1.0 g, 5.0 mmol) in EtOH (20 mL) was added hydroxylamine hydrochloride (0.365 g, 5.0 mmol) and NaOH (0.212 g, 5.0 mmol). The resulting reaction mixture was refluxed for 15 h. After the completion of the reaction (TLC monitoring), the mixture was concentrated, added EtOH and filtered. The filtrate was evaporated in vacuo and used as such for the next step (crude yield 12.0 g, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088791B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-c8d553a8b896403caea3eda8a9e78ae2 |
| Source note | uspto-grants-2012_01 |