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 | Triethylamine | HCID 8471 | — |
| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Acetamide, N-(3-methoxyphenyl)- | HCID 11494 | — |
Reaction Steps
120 ml of triethylamine and 56.7 ml of acetic anhydride were added dropwise to a stirred solution of 70.5 g of m-anisidine in 500 ml of a methylene chloride under ice cooling. After completion of the dropwise addition, the reaction mixture was washed and dried, and insolubles were filtered off. The filtrate was concentrated, and the residue was recrystallized from hexane-ethyl acetate to afford 80.9 g of N-(3-methoxyphenyl)acetamide as pale yellow needles. Melting point: 81° to 82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05807883 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-7efb6f77258d43bbb6260c85d57de67c |
| Source note | uspto-grants-1998_09 |