Ethyl Acetate → HCID 21846284, 화합물
반응식
[C:1]([C:4]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:5]=1[CH:6]=[CH:7][NH:8]2)(=[O:3])[CH3:2].[H-].[Na+].[C:15](OCC)(=[O:17])[CH3:16]>>[NH:8]1[C:9]2[C:5](=[C:4]([C:1](=[O:3])[CH2:2][C:15](=[O:17])[CH3:16])[CH:12]=[CH:11][CH:10]=2)[CH:6]=[CH:7]1참가 물질
4
실험 절차
4-Acetylindole (0.101 g) was refluxed in 5 mL of ethyl acetate. Sodium hydride (0.20 g, 60% oil dispersion) was added in portions to the refluxing solution until thin layer chromatography analysis showed complete consumption of the starting material. The reaction mixture was quenched with water and acidified to pH 3. The ethyl acetate layer was dried (magnesium sulfate) and concentrated to give a crude product. The crude material was chromatographed on silica gel, eluting with hexane/ethyl acetate to give 1-(1H-indol-4-yl)-1,3-butanedione (0.104 g), a compound of formula (11), m.p. 104-105° C.
후처리
- customconsumption of the starting material
- customThe reaction mixture was quenched with water
- dry with materialThe ethyl acetate layer was dried (magnesium sulfate)
- concentrationconcentrated
- customto give a crude product
- customThe crude material was chromatographed on silica gel
- washeluting with hexane/ethyl acetate
출처 및 근거
- ORD 기록
- ord-3e825c4744c24e299eecd3f54913631f
- 출처 데이터셋
- uspto-grants-1999_09
- 특허 번호
- US05958934
반응 노트
불러오는 중…