반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH2:9])=[C:5]([CH3:10])[CH:4]=1.CN(C)CC.[C:16](OC(=O)C)(=[O:18])[CH3:17]>O1CCCC1>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:16](=[O:18])[CH3:17])=[C:5]([CH3:10])[CH:4]=1참가 물질
5
반응 조건
- 온도
- 0 °C
실험 절차
41.1 g (0.3 mol) of 4-methoxy-2-methylphenylamine and 37 g (0.5 mol) of dimethylethylamine were dissolved in 50 ml of tetrahydrofuran, and 35.7 g (0.35 mol) of acetic anhydride were added while stirring. The solution heated to boiling during this. It was stirred at room temperature for 1 hour and cooled to 0° C. The resulting precipitate was filtered off with suction and washed several times with a little cold tetrahydrofuran and dried. 40 g (75%) of colorless crystals of the desired product were obtained.
후처리
- temperatureThe solution heated
- stirringIt was stirred at room temperature for 1 hour
- filtrationThe resulting precipitate was filtered off with suction
- washwashed several times with a little cold tetrahydrofuran
- customdried
출처 및 근거
- ORD 기록
- ord-79359b97dd9445d7817107dff3c837b9
- 출처 데이터셋
- uspto-grants-2012_08
- 특허 번호
- US08247452B2
연결된 노트
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