HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(3-fluoro-2-methylphenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Fluoro-2-methylaniline | HCID 285553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-fluoro-2-methylphenyl)acetamide | HCID 1489284 | — |
Reaction Steps
1-amino-3-fluoro-2-methylbenzene (1 equivalent) was dissolved in CH2Cl2 and acetic anhydride (2.0 equivalents) was added slowly. The solution was stirred at room temperature for 4 hours. The reaction mixture was then quenched with water, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with H2O, a 10% HCl solution, H2O, and brine. It was then dried over Na2SO4 and concentrated in vacuo, to yield N-(3-fluoro-2-methylphenyl)acetamide as a pink solid. LC/MS (m/z) 168.2 (MH+), Rt 1.91 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07064215B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-8238e89799944c5694d8826358b1f0d3 |
| Source note | uspto-grants-2006_06 |