2-Methylpyridine → 1-[4-(4-Butyl-phenyl)-butyl]-2-methyl-pyridinium bromide

HRID 84329

反応式

HRID 84329 の反応式
[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][CH:19]=[CH:18][C:17]=1[CH3:22]>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][CH:19]=[CH:18][C:17]=2[CH3:22])=[CH:7][CH:8]=1)[CH2:13][CH2:14][CH3:15]

参加物

4

反応物 2

HCID 79752-MethylpyridineHCID 198479361-(4-Bromo-butyl)-4-butyl-benzene

生成物 1

HCID 247807931-[4-(4-Butyl-phenyl)-butyl]-2-methyl-pyridinium bromide収率 74%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

1-(4-Bromo-butyl)-4-butyl-benzene (1 mmol) was added to a solution of 2-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 2-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 (74%). 1HNMR (300 MHz, CDCl3, ppm), 9.69 (d, J=6.6, 1H), 8.25-8.30 (m, 1H), 7.90-7.95 (m, 1H), 7.77 (d, J=7.8, 1H), 7.04-7.10 (m, 4H), 4.92 (t, 7.5, 2H), 2.84 (s, 3H), 2.66 (t, J=7.2, 2H), 2.56 (t, J=7.5, 2H), 1.89-1.98 (m, 2H), 1.78-1.86 (m, 2H), 1.51-1.59 (m, 2H), 1.27-1.37 (m, 2H), 0.91 (t, J=7.2, 3H).

後処理

  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 2-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

出典と根拠

ORDレコード
ord-e73286bb591c41babb7e27e49179d8e4
出典データセット
uspto-grants-2014_09
特許番号
US08846937B2

関連ノート

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