Butyl iodide → 3-Butyl-2,4,5-trimethylthiazol-3-ium iodide
反応式
[CH3:1][C:2]1[S:3][C:4]([CH3:8])=[C:5]([CH3:7])[N:6]=1.[CH2:9]([I:13])[CH2:10][CH2:11][CH3:12]>C(#N)C>[I-:13].[CH2:9]([N+:6]1[C:5]([CH3:7])=[C:4]([CH3:8])[S:3][C:2]=1[CH3:1])[CH2:10][CH2:11][CH3:12]参加物
4
実験手順
A mixture of 2,4,5-trimethylthiazole (1.3 g, 10 mmol) and n-butyl iodide (7.4 g, 40 mmol) in anhydrous acetonitrile (30 mL) was refluxed for 72 hours and then concentrated under reduced pressure to provide the crude thiazolium salt. 1H NMR (300 MHz, DMSO-d6) δ 0.95 (t, J=7 Hz, 3H), 1.39 (sextet, J=7 Hz, 2H), 1.65 (m, 2H), 2.43 (s, 6H), 2.96 (s, 3H), 4.25 (m, 2H).
後処理
- temperaturewas refluxed for 72 hours
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-20b9fb863e514c1190cbe561ccf3576c
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08481574B2
反応ノート
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