Methyl iodide → Ethyl 2-(pyridin-4-yl)propanoate
反応式
[Li]N([Si](C)(C)C)[Si](C)(C)C.[N:11]1[CH:16]=[CH:15][C:14]([CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])=[CH:13][CH:12]=1.[CH3:23]I>C1COCC1>[N:11]1[CH:16]=[CH:15][C:14]([CH:17]([CH3:23])[C:18]([O:20][CH2:21][CH3:22])=[O:19])=[CH:13][CH:12]=1参加物
5
実験手順
To a solution of LiN(TMS)2 (Aldrich, 1.0 M solution in THF, 30 mL, 30 mmol) in THF (30 mL) was added ethyl 4-pyridylacetate (Aldrich, 4.7 mL, 30 mmol)) at 0° C. Methyl iodide (Aldrich, 2.4 mL, 38 mmol) was added 30 min later. After 1 h, the reaction mixture was concentrated in vacuo. The crude product was purified by silica gel chromatography. Mass Spec. m/z+ion 180 (M+1).
後処理
- concentrationthe reaction mixture was concentrated in vacuo
- customThe crude product was purified by silica gel chromatography
出典と根拠
- ORDレコード
- ord-7b348aade2a44a4897ead385b0bf66b6
- 出典データセット
- uspto-grants-2010_10
- 特許番号
- US07807700B2
反応ノート
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