Dimethylamine → 2-((Dimethylamino)methyl)-4-fluorobenzonitrile
反応式
Br[CH2:2][C:3]1[CH:10]=[C:9]([F:11])[CH:8]=[CH:7][C:4]=1[C:5]#[N:6].[CH3:12][NH:13][CH3:14]>>[CH3:12][N:13]([CH2:2][C:3]1[CH:10]=[C:9]([F:11])[CH:8]=[CH:7][C:4]=1[C:5]#[N:6])[CH3:14]参加物
3
実験手順
A mixture of 2-(bromomethyl)-4-fluorobenzonitrile (423 mg, 1.9 mmol) and 2.0 M dimethylamine (4 mL) was stirred at room temperature for thirty minutes. The mixture was then concentrated, purified by normal phase flash column chromatography, on a 20 g silica gel column (5-45% ethyl acetate/hexanes gradient), and concentrated in vacuo to yield 2-((dimethylamino)methyl)-4-fluorobenzonitrile (241 mg, 1.35 mmol, 68%). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.92 (dd, J=8.59, 5.37 Hz, 1H), 7.42 (dd, J=9.94, 2.69 Hz, 1H), 7.35 (td, J=8.46, 2.69 Hz, 1H), 3.56 (s, 2H), 2.19 (s, 6H).
後処理
- concentrationThe mixture was then concentrated
- custompurified by normal phase flash column chromatography, on a 20 g silica gel column (5-45% ethyl acetate/hexanes gradient)
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-244643bb5fc3449883688905ff3ffdfb
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07781428B2
反応ノート
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