반응식
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:8]=[CH:7][C:6]([C:9](=[O:11])[CH3:10])=[CH:5][CH:4]=1.CO[C:16]([N:20]([CH3:22])[CH3:21])(OC)[CH3:17]>C(OCC)C>[CH3:21][N:20]([CH3:22])[C:16]([CH3:17])=[CH:10][C:9]([C:6]1[CH:5]=[CH:4][C:3]([C:2]([F:12])([F:13])[F:1])=[CH:8][CH:7]=1)=[O:11]참가 물질
4
반응 조건
- 온도
- 112 °C
실험 절차
A mixture of 4′-(trifluoromethyl)acetophenone (9.8 g) and N-(1,1-dimethoxyethyl)-N,N-dimethylamine (8.2 g) was heated at 112° C. overnight, under nitrogen. The reaction mixture was cooled and concentrated giving an orange solid. Trituration with diethyl ether gave the title compound as a yellow solid
후처리
- temperatureThe reaction mixture was cooled
- concentrationconcentrated
- customgiving an orange solid
출처 및 근거
- ORD 기록
- ord-1ea84c7acf084517a9e9625c59ac88bf
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07091237B2
연결된 노트
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