반응식
[CH2:1]([O:3][C:4]([C:6]1([C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH2:10][CH:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[N+:17]([O-])=O)[CH:8](O)[N:7]1[CH:21]=[O:22])=[O:5])[CH3:2].CO.[H][H]>[Ni].C(O)(=O)C>[CH2:1]([O:3][C:4](=[O:5])[C:6]([NH:7][CH:21]=[O:22])([C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH2:10][C:9]1[C:11]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[NH:17][CH:8]=1)[CH3:2]참가 물질
실험 절차
50.0 g (0.13 mol) of the compound of Example 4 in 500 ml. of methanol and 1 ml of acetic acid was hydrogenated in a rocking autoclave at room temperature and 200 psi in the presence of 6 g. of Raney nickel. After the hydrogen uptake (3 equivalents) was complete the filtered reaction mixture was concentrated in vacuo to a volume of 140 ml. Toluene (600 ml.) was added and the remaining methanol was removed by azeotropic distillation. The mixture was heated at reflux for an additional 30 minutes and then allowed to cool to room temperature. The precipitate was collected, washed with toluene and dried to yield 42.3 g (97%) of white crystals, m.p. 179-180° (lit. m.p. 179°). The analytical sample was prepared by recrystallization from ethaniol: m.p. 180-181°.
후처리
- customwas hydrogenated in a rocking autoclave at room temperature
- customthe filtered reaction mixture
- concentrationwas concentrated in vacuo to a volume of 140 ml
- additionToluene (600 ml.) was added
- customthe remaining methanol was removed by azeotropic distillation
- temperatureThe mixture was heated
- temperatureat reflux for an additional 30 minutes
- customThe precipitate was collected
- washwashed with toluene
- customdried
출처 및 근거
- ORD 기록
- ord-b74a3c1de5cf4d8186054f1480f7ec75
- 출처 데이터셋
- uspto-grants-1979_02
- 특허 번호
- US04140697
연결된 노트
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