반응식
C1(C)C=CC=CC=1.[NH2:8][CH2:9][CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][NH:11]1.O.[F:17][C:18]([F:42])([F:41])[CH2:19][O:20][C:21]1[CH:34]=[CH:33][C:32]([O:35][CH2:36][C:37]([F:40])([F:39])[F:38])=[CH:31][C:22]=1[C:23](OCC(F)(F)F)=[O:24]>CO>[CH:33]1[C:32]([O:35][CH2:36][C:37]([F:38])([F:39])[F:40])=[CH:31][C:22]([C:23]([NH:8][CH2:9][CH:10]2[NH:11][CH2:12][CH2:13][CH2:14][CH2:15]2)=[O:24])=[C:21]([O:20][CH2:19][C:18]([F:17])([F:41])[F:42])[CH:34]=1참가 물질
반응 조건
- 온도
- 50 °C
실험 절차
Dissolve in 48 ml of toluene 12.0 g (0.03 mol) of trifluoroethanol 2,5-bis-trifluoroethoxybenzoate. Add 3.94 g (0.0345 mol) of 2-aminomethylpiperidine and heat the solution to a temperature of 80°±5° C. for 8 hours. Cool to 50° C. and add 36 ml of water. Carry out the separation at a temperature of 45°±5° C. Concentrate the organic phase under vacuum at a temperature of 35°±5° C. so as to eliminate as much toluene as possible. A semi-solid residue is obtained which is dissolved in 20 ml of methanol and concentrated again to a residue under vacuum. Methanol (40 ml) is then added and heated with refluxing until a yellow solution is obtained. Then cool until the crude base crystallizes, the precipitation is completed by adding 40 ml of water.
후처리
- temperatureheat the solution to a temperature of 80°±5° C. for 8 hours
- customCarry out the separation at a temperature of 45°±5° C
- concentrationConcentrate the organic phase under vacuum at a temperature of 35°±5° C. so as
- customA semi-solid residue is obtained which
- concentrationconcentrated again to a residue under vacuum
- additionMethanol (40 ml) is then added
- temperatureheated
- temperaturewith refluxing until a yellow solution
- customis obtained
- customcrystallizes
- customthe precipitation
- additionby adding 40 ml of water
출처 및 근거
- ORD 기록
- ord-fd062efa44324b67b5831a945dd1e406
- 출처 데이터셋
- uspto-grants-2003_07
- 특허 번호
- US06599922B2
연결된 노트
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