반응식
O.[NH2:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([OH:13])=[CH:5][CH:4]=1.[C:14](OC(=O)C)(=[O:16])[CH3:15]>C(O)C>[OH:13][C:6]1[C:7]2[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:3]([NH:2][C:14](=[O:16])[CH3:15])=[CH:4][CH:5]=1참가 물질
5
실험 절차
Into a 500 ml round bottom flask (fitted with a magnetic stirrer), a 50:50 mixture of water:ethanol was combined with 4-amino1-naphthol (20 g, 125 mmole) until the solid was completely dissolved. The solution was warmed to boiling, and to it was added acetic anhydride (14 g) and the resulting solution was stirred for 1 hour. Upon cooling, crystals of N-(4-hydroxy-1-naphthyl)acetamide (20 g, 79% yield) formed.
후처리
- customInto a 500 ml round bottom flask (fitted with a magnetic stirrer)
- dissolutionwas completely dissolved
- temperatureThe solution was warmed
- temperatureUpon cooling
출처 및 근거
- ORD 기록
- ord-9d36a4eb96e4449bbcd6f139e87e7d73
- 출처 데이터셋
- uspto-grants-1994_12
- 특허 번호
- US05372931
연결된 노트
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