Thionyl Chloride → Benzimidazole, 1-(4-chlorobutyl)-

HRID 354945

反応式

HRID 354945 の反応式
[N:1]1([CH2:10][CH2:11][CH2:12][CH2:13]O)[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1.S(Cl)([Cl:17])=O>ClC(Cl)Cl>[Cl:17][CH2:13][CH2:12][CH2:11][CH2:10][N:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1

参加物

4

反応物 2

HCID 24386Thionyl ChlorideHCID 205063231h-Benzimidazole-1-butanol

生成物 1

HCID 583170Benzimidazole, 1-(4-chlorobutyl)-

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

To a stirred mixture of 50 parts of 1H-benzimidazole-1-butanol and 375 parts of trichloromethane are added dropwise 35.2 parts of sulfinyl chloride. Upon completion, stirring is continued for 3 hours at reflux temperature. The reaction mixture is evaporated. The residue is taken up in trichloromethane. The whole is washed with ammonium hydroxide and the solvent is evaporated. The residue is purified by column-chromatography over silica gel using trichloromethane as eluent. The pure fractions are collected and the eluent is evaporated, yielding 1-(4-chlorobutyl)-1H-benzimidazole as an oily residue.

後処理

  1. temperatureat reflux temperature
  2. customThe reaction mixture is evaporated
  3. washThe whole is washed with ammonium hydroxide
  4. customthe solvent is evaporated
  5. customThe residue is purified by column-chromatography over silica gel
  6. customThe pure fractions are collected
  7. customthe eluent is evaporated

出典と根拠

ORDレコード
ord-eae46e8a18d849acb1dea969723bbdb2
出典データセット
uspto-grants-1983_03
特許番号
US04377578

関連ノート

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