Tetrabutylammonium Fluoride → 2-Chloro-5-ethynylpyridine
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[C:9][Si](C)(C)C)=[CH:4][N:3]=1.[F-].C([N+](CCCC)(CCCC)CCCC)CCC>C1COCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[CH:9])=[CH:4][N:3]=1参加物
4
実験手順
2-Chloro-5-trimethylsilanylethynyl-pyridine (1.00 g, 4.77 mmol) was taken up in THF (23.8 ml) under argon at 0° C. Tetrabutylammonium fluoride (5.72 ml of 1.0 M in THF, 5.72 mmol) was added dropwise over 5 minutes. The mixture was then allowed to warm to room temperature and maintained at room temperature for 1.5 hours. The reaction was quenched with saturated aqueous ammonium chloride, and extracted three times with ethyl acetate. The organic fractions were combined, dried over anhydrous magnesium sulfate, filtered, and concentrated. The resulting crude product was purified by silica gel chromatography (0-65% ethyl acetate/hexanes) to afford the title compound.
後処理
- temperaturemaintained at room temperature for 1.5 hours
- customThe reaction was quenched with saturated aqueous ammonium chloride
- extractionextracted three times with ethyl acetate
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe resulting crude product was purified by silica gel chromatography (0-65% ethyl acetate/hexanes)
出典と根拠
- ORDレコード
- ord-0ea4ea62381b4707b1f2c1f149774f11
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08367706B2
反応ノート
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