Sodium Carbonate → 1-(2'-Hexyldecyl)-2-ethyl-4,5,6,7-tetrahydrobenzimidazole

HRID 249222ノート

反応式

HRID 249222 の反応式
[CH2:1]([C:3]1[NH:4][C:5]2[CH2:11][CH2:10][CH2:9][CH2:8][C:6]=2[N:7]=1)[CH3:2].Br[CH2:13][CH:14]([CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22].C(=O)([O-])[O-].[Na+].[Na+]>COCCO>[CH2:23]([CH:14]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])[CH2:13][N:7]1[C:6]2[CH2:8][CH2:9][CH2:10][CH2:11][C:5]=2[N:4]=[C:3]1[CH2:1][CH3:2])[CH2:24][CH2:25][CH2:26][CH2:27][CH3:28]

参加物

5

実験手順

2-Ethyl-4,5,6,7-tetrahydrobenzimidazole (14.3 parts), 2-methoxyethanol (30 parts), 1-bromo-2-hexyldecane (35 parts) and sodium carbonate (5.7 parts) are stirred together and heated at 125°-135° C. below a reflux condenser for 15 hours. The reaction mixture is cooled and extracted with a mixture of toluene (150 parts) and ethyl acetate (50 parts) and the extract is washed successively with water, dilute sulphuric acid, dilute sodium hydroxide, and water, and then distilled yielding 1-(2'-hexyldecyl)-2-ethyl-4,5,6,7-tetrahydrobenzimidazole (V) (16.6 parts), b.p. 185°-200° at 0.2 mm pressure.

後処理

  1. temperatureheated at 125°-135° C. below a reflux condenser for 15 hours
  2. temperatureThe reaction mixture is cooled
  3. extractionextracted with a mixture of toluene (150 parts) and ethyl acetate (50 parts)
  4. washthe extract is washed successively with water, dilute sulphuric acid, dilute sodium hydroxide, and water
  5. distillationdistilled

出典と根拠

ORDレコード
ord-e455e2f537164ad0883c7d0302fc97e0
出典データセット
uspto-grants-1993_05
特許番号
US05213777

反応ノート

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