참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | 2,5-Difluoro-4-nitroaniline | HCID 235930 | — |
| 촉매 | Sulfuric Acid | HCID 1118 | — |
| 촉매 | 2-Dimethylaminopyridine | HCID 21885 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(2,5-Difluoro-4-nitrophenyl)acetamide | HCID 14624893 | 88.4% |
반응 단계
A mixture of 6.0 g (0.034 mole) of 2,5-difluoro-4-nitroaniline, 6.5 g (0.064 mole) of acetic anhydride, and approximately 0.1 g (0.0008 mole) of dimethylaminopyridine in 300 ml of methylene chloride was stirred and heated at reflux for two hours. The reaction mixture was allowed to cool and stir at room temperature for approximately 18 hours. The solvent was removed from the mixture by distillation under reduced pressure, leaving a residue. To this residue was added 32.5 g (0.318 mole) of acetic anhydride and several drops of concentrated sulfuric acid. This mixture was stirred at room temperature for approximately 18 hours. Approximately 300 ml of water was added to the mixture causing a vigorous exotherm and a solid to form. This solid was collected by filtration. The filter cake was washed with water and was dried under reduced pressure to yield 6.5 g of N-(2,5-difluoro-4-nitrophenyl)acetamide. The nmr spectrum was consistent with the proposed structure.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05310724 |
|---|
| 출처 데이터셋 | uspto-grants-1994_05 |
|---|
| ORD ID | ord-577bd73ef8644ddb9ec7a279ccfeae41 |
|---|
| 출처 메모 | uspto-grants-1994_05 |
|---|