Sodium hydride → 2-(2-Fluoro-phenyl)-cyclopropanecarboxylic acid methoxy-methyl-amide
반응식
[H-].[Na+].[I-].[CH3:4][S+](C)(C)=O.[F:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[CH:16]=[CH:17][C:18]([N:20]([O:22][CH3:23])[CH3:21])=[O:19]>CN(C=O)C>[CH3:23][O:22][N:20]([CH3:21])[C:18]([CH:17]1[CH2:4][CH:16]1[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[F:9])=[O:19]참가 물질
실험 절차
NaH (8 g, 60% oil dispersion) was added to a suspension of trimethylsulfoxonium iodide (44 g) in DMF (150 mL) at 0° C. The resulting mixture was allowed to warm to room temperature and stirred for 0.5 h. A solution of 3-(2-fluoro-phenyl)-N-methoxy-N-methyl-acrylamide (19.5 g) was added to the above reaction mixture at 0° C., and the resulting reaction was allowed to warm to room temperature and stirred for 2 h. The reaction was quenched with water and the aqueous layer was extracted with CH2Cl2. The combined organic layers were washed with brine, dried over MgSO4, and concentrated in vacuo to give a residue. The residue was purified by flash chromatography over silica gel (elution with 50% hexanes in ethyl acetate) to give the title compound (16 g) as an oil.
후처리
- customthe resulting reaction
- temperatureto warm to room temperature
- stirringstirred for 2 h
- customThe reaction was quenched with water
- extractionthe aqueous layer was extracted with CH2Cl2
- washThe combined organic layers were washed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customto give a residue
- customThe residue was purified by flash chromatography over silica gel (elution with 50% hexanes in ethyl acetate)
출처 및 근거
- ORD 기록
- ord-ba2d9ff610634dbea4c5253658474c71
- 출처 데이터셋
- uspto-grants-2006_12
- 특허 번호
- US07144881B2
반응 노트
불러오는 중…