Tetrahydrofuran → 6-(Methylthio)nicotinonitrile
반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([C:8]#[N:9])=[CH:4][N:3]=1.[CH3:10][S-:11].[Na+].C1COCC1.C(OCC)(=O)C>O>[C:8]([C:5]1[CH:6]=[CH:7][C:2]([S:11][CH3:10])=[N:3][CH:4]=1)#[N:9]참가 물질
6
실험 절차
2-Chloro-5-cyanopyridine (2.10 g, 15.1 mmol) and sodium thiomethoxide (1.16 g, 16.5 mmol) were added to THF (30 ml). The reaction mixture was refluxed for 9 hrs and combined with ethyl acetate and water. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated to give the titled compound (2.26 g, 100%) as pale yellow crystals.
후처리
- temperatureThe reaction mixture was refluxed for 9 hrs
- washThe organic layer was washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent was evaporated
출처 및 근거
- ORD 기록
- ord-7919732e7ebf405dba9b80d1ec3b1d07
- 출처 데이터셋
- uspto-grants-2008_07
- 특허 번호
- US07399759B2
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