반응식
[C:1]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=O)[CH2:2][CH2:3][CH3:4].[NH:12]1[CH2:16][CH2:15][CH2:14][CH2:13]1.B(F)(F)F.CCOCC.O>C1(C)C=CC=CC=1>[C:6]1([C:1]([N:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)=[CH:2][CH2:3][CH3:4])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1참가 물질
6
실험 절차
In 50 ml of toluene, 4.44 g of n-butyrophenone, 6.40 g of pyrrolidine and 0.43 g of boron trifluoride etherate were dissolved. The mixture was refluxed for 47 hours using a Cope water separator and molecular sieve 4A as the dehydrating agent. After having distilled out the solvent under a reduced pressure, the residue was subjected to a distillation under a reduced pressure to obtain the desired enamine as a pale yellowish oil (yield: 4.66 g, 77%).
후처리
- temperatureThe mixture was refluxed for 47 hours
- distillationAfter having distilled out the solvent under a reduced pressure
- distillationthe residue was subjected to a distillation under a reduced pressure
출처 및 근거
- ORD 기록
- ord-d197b6ee4eb349e0a26ef7b41d5e3423
- 출처 데이터셋
- uspto-grants-1980_04
- 특허 번호
- US04198510
연결된 노트
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