4-甲基吡啶 → 1-[4-(4-Butyl-phenyl)-butyl]-4-methyl-pyridinium bromide

HRID 84331笔记

反应方程式

HRID 84331 反应方程式
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][CH2:13][CH2:14][CH3:15])=[CH:8][CH:7]=1.[N:16]1[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][CH:17]=1>C(#N)C>[Br-:1].[CH2:12]([C:9]1[CH:10]=[CH:11][C:6]([CH2:5][CH2:4][CH2:3][CH2:2][N+:16]2[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][CH:17]=2)=[CH:7][CH:8]=1)[CH2:13][CH2:14][CH3:15]

参与物

4

实验过程

1-(4-Bromo-butyl)-4-butyl-benzene (1 mmol) was added to a solution of 4-picoline (3 mmol) in acetonitrile, and the solution was refluxed for 24 hours. The acetonitrile was removed in a vacuum, and the resulting residue was partitioned between ether and water. The aqueous layer was washed extensively with ether until no picoline was left in the aqueous layer. The resulting aqueous solution of the product was extracted with chloroform. The chloroform was removed to afford the product (72%). 1HNMR (300 MHz, CDCl3, ppm), 9.22 (d, J=6.6, 2H), 7.79 (d, J=6.6, 2H), 7.05 (d, J=8.4, 2H), 7.02 (d, J=8.4, 2H), 4.90 (t, J=7.5, 3H), 2.51-2.63 (m, 7H), 1.96-2.06 (m, 2H), 1.58-1.68 (m, 2H), 1.51-1.61 (m, 2H), 1.31-1.37 (m, 2H), 0.89 (t, J=7.2, 3H); 13CNMR, 158.91, 144.31, 140.83, 138.30, 128.92, 128.66, 128.45, 61.26, 35.54, 34.95, 34.04, 31.61, 27.95, 22.73, 22.57, 14.33.

后处理

  1. temperaturethe solution was refluxed for 24 hours
  2. customThe acetonitrile was removed in a vacuum
  3. customthe resulting residue was partitioned between ether and water
  4. washThe aqueous layer was washed extensively with ether until no picoline
  5. waitwas left in the aqueous layer
  6. extractionThe resulting aqueous solution of the product was extracted with chloroform
  7. customThe chloroform was removed

来源与证据

ORD记录
ord-61b3f1a1ee324191a4e463deb7be134f
来源数据集
uspto-grants-2014_09
专利号
US08846937B2

反应笔记

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