HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Acetamide, N-(3-methoxyphenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Acetamide, N-(3-methoxyphenyl)- | HCID 11494 | 96.4% |
Reaction Steps
To a stirred solution of m-anisidine (12.3 g, 0.1 mol) in THF (80 mL) was added acetic anhydride (11.3 mL, 0.12 mol) at 0° C. The mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with water (50 mL), brine (30 mL), dried over MgSO4, and concentrated in vacuo. The resulting solid was recrystallized from methylene chloride-hexane to give the subtitle compound (15.9 g, 96.4% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608095B2 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-1f9facf764844d6084e545ef14107461 |
| Source note | uspto-grants-2003_08 |