3-Methylpyridine → 3-Methyl-1-(8-phenyl-octyl)-pyridinium bromide

HRID 84317

反応式

HRID 84317 の反応式
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[N:16]1[CH:21]=[CH:20][CH:19]=[C:18]([CH3:22])[CH:17]=1>C(#N)C>[Br-:1].[CH3:22][C:18]1[CH:17]=[N+:16]([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:21]=[CH:20][CH:19]=1

参加物

4

反応物 2

HCID 79703-MethylpyridineHCID 563758(8-Bromooctyl)benzene

生成物 1

HCID 247811053-Methyl-1-(8-phenyl-octyl)-pyridinium bromide収率 76%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

(8-Bromo-octyl)-benzene (1 mmol) was added to a solution of 3-picoline (3 mmol) in acetonitrile, and the solution 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 (76%). 1HNMR (300 MHz, CDCl3, ppm) 9.40 (s, 1H), 9.22 (d, 1H), 8.02 (d, 1H), 7.96 (dd, 1H), 7.12-7.22 (dd, 4H), 4.94 (t, 2H), 2.62 (s, 3H), 2.56 (t, 2H), 1.94-2.04 (m, 2H), 1.50-1.60 (m, 2H), 1.20-1.40 (br, 8H). 13CNMR, 145.68, 144.65, 142.87, 142.37, 139.79, 128.55, 128.40, 127.89, 125.76, 62.20, 36.19, 32.29, 31.73, 29.53, 29.44, 29.33, 26.40, 19.11.

後処理

  1. temperaturethe solution 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

出典と根拠

ORDレコード
ord-a965aae1bccb46a0be0204f2cd58c0ab
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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