HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → n-(2,5-difluorophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2,5-Difluoroaniline | HCID 67775 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | n-(2,5-difluorophenyl)acetamide | HCID 242830 | 94.2% |
Reaction Steps
20.5 g of 2,5-difluoroaniline was dissolved in 68 ml of benzene, and 17.8 g of acetic anhydride was dropwise added. Fifteen hours later, benzene was distilled off, and the residue was washed with ethyl ether to obtain 25.6 g of 2,5-difluoroacetanilide as white crystals. Then, this compound was dissolved in 98% sulfuric acid, and 60% nitric acid was dropwise added at a temperature of not higher than 0° C. After the dropwise addition, the mixture was stirred for three hours at room temperature, and poured on ice. Precipitated crystals were collected by filtration and dried to obtain 25.9 g of the above-identified compound as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05039331 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-211ebb41bcad4b99b1f3d0063dcdc009 |
| Source note | uspto-grants-1991_08 |