HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → N-(4-Methoxyphenyl)Acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Hexane | HCID 8058 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-Methoxyphenyl)Acetamide | HCID 5827 | 92.7% |
Reaction Steps
Acetic anhydride (10.21 g, 9.4 mL, 100 mmol) was added dropwise over 1 hour to a stirred solution of p-anisidine (12.32 g, 100 mmol) in dichloromethane (40 mL) at 25-30° C. The mixture was stirred for an additional 1 hour at the same temperature. Hexane (120 mL) was added dropwise to the mixture at 25-30° C. The obtained suspension was stirred for 1 hour at the same temperature. The precipitated crystals were separated by filtration and dried under reduced pressure to give 15.31 g (92.7%) of N-(4-methoxyphenyl)acetamide [3a] as off-white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07312345B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-38322b5735724350b04435a1314156df |
| Source note | uspto-grants-2007_12 |