반응식
[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=O)[C:5]2=[O:12].[OH-:13].[Na+].C(OCC([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)=O)(=O)C.[CH2:34]([OH:36])[CH3:35]>O>[OH:12][C:5]1[C:6]([C:26]2[CH:25]=[CH:24][C:23]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)=[CH:22][CH:27]=2)=[N:7][C:8]2[C:4]([C:35]=1[C:34]([OH:13])=[O:36])=[CH:3][C:2]([CH3:1])=[CH:10][CH:9]=2참가 물질
실험 절차
A mixture of 30 g of 5-methyl-2,3-indolinedione in 200 ml of water and 30.6 g of sodium hydroxide in 100 ml of water was reacted with a solution of 47.4 g of acetoxyacetylbiphenyl in 500 ml of ethanol. The mixture was refluxed for 3 hours, then 250 ml of ethanol was removed by distillation. A 500 ml portion of water was added, The mixture was stirred, cooled to room temperature and filtered through diatomaceous earth. The filtrate was acidified with 60 ml of concentrated hydrochloric acid and 20 ml of glacial acetic acid. The resulting solid was collected, taken up in dilute ammonia and the insoluble portion collected. This solid was dissolved in 7.4N ammonia, filtered and precipitated with glacial acetic acid, giving 32.0 g of the desired product, mp 236°-238° C.
후처리
- temperatureThe mixture was refluxed for 3 hours
- custom250 ml of ethanol was removed by distillation
- additionA 500 ml portion of water was added
- filtrationfiltered through diatomaceous earth
- customThe resulting solid was collected
- customthe insoluble portion collected
- dissolutionThis solid was dissolved in 7.4N ammonia
- filtrationfiltered
- customprecipitated with glacial acetic acid
출처 및 근거
- ORD 기록
- ord-17d4ac50c57b4598a3bd803118256f0b
- 출처 데이터셋
- uspto-grants-1989_07
- 특허 번호
- US04847381
연결된 노트
불러오는 중…