p-Toluenesulfonic acid → 1-Propanone, 1-(2,4-difluorophenyl)-2-[(tetrahydro-2H-pyran-2-YL)oxy]-,(2R)-
반응식
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:13])[CH:10]([OH:12])[CH3:11].C1(C)C=CC(S(O)(=O)=O)=CC=1.[O:25]1[CH:30]=[CH:29][CH2:28][CH2:27][CH2:26]1.C(=O)([O-])O.[Na+]>C(Cl)Cl>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:13])[CH:10]([O:12][CH:26]1[CH2:27][CH2:28][CH2:29][CH2:30][O:25]1)[CH3:11]참가 물질
실험 절차
2',4'-Difluoro-2-hydroxypropiophenone (61 g) was dissolved in methylene chloride (500 ml), to which was added, under ice-cooling, p-toluene sulfonic acid.hydrate (1.0 g). To the mixture was added, under ice-cooling while stirring, 3,4-dihydro-2H-pyran (41.4 g) during 10 minutes. The mixture was stirred, under ice-cooling, for one hour, to which was added a 5% aqueous solution of sodium hydrogen carbonate (240 ml). The mixture was stirred for 10 minutes under ice-cooling. The methylene chloride layer was separated and dried over anhydrous magnesium sulfate, followed by distilling off the solvent. The residual oily product was purified by means of a silica gel column chromatography (hexane: ethyl acetate=5:1) to afford 2',4'-difluoro-2-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)propiophenone (86.5 g) as a pale yellow oily product.
후처리
- additionwas added, under ice-
- temperaturecooling
- additionTo the mixture was added, under ice-
- temperaturecooling
- stirringThe mixture was stirred, under ice-
- temperaturecooling, for one hour, to which
- stirringThe mixture was stirred for 10 minutes under ice-
- temperaturecooling
- customThe methylene chloride layer was separated
- dry with materialdried over anhydrous magnesium sulfate
- distillationby distilling off the solvent
- customThe residual oily product was purified by means of a silica gel column chromatography (hexane: ethyl acetate=5:1)
출처 및 근거
- ORD 기록
- ord-470f5ff8c17b447f8c8e2ffbda035a00
- 출처 데이터셋
- uspto-grants-1995_04
- 특허 번호
- US05405861
반응 노트
불러오는 중…