HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(5-Bromo-2-(trifluoromethoxy)phenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-Bromo-2-(trifluoromethoxy)aniline | HCID 2779367 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(5-Bromo-2-(trifluoromethoxy)phenyl)acetamide | HCID 3603102 | 95% |
Reaction Steps
To a solution of 2-trifluoromethoxy-5-bromo-phenylamine (5.12 g, 20 mmol) in EtOH (50 mL) at 0° C. was added a solution of acetic anhydride (4.7 mL, 50 mmol) in EtOH (10 mL). The mixture was stirred at room temperature overnight. The solvent was evaporated to dryness and the solid was tritured with diethyl ether and filtered to give 5.64 g (95% yield) of N-(5-bromo-2-trifluoromethoxy-phenyl)-acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426417B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-aa2f9b45f5cb49ad8c1e227a48e80be9 |
| Source note | uspto-grants-2013_04 |