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Triethylamine → 2-(4-Chlorobutylthio)pyridine

HRID 6172
ノート
印刷プレビュー

反応式

HRID 6172 の反応式
[SH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.C(N(CC)CC)C.Br[CH2:16][CH2:17][CH2:18][CH2:19][Cl:20]>C(O)C>[Cl:20][CH2:19][CH2:18][CH2:17][CH2:16][S:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8471TriethylamineHCID 813641-Bromo-4-chlorobutaneHCID 178418616HCID 178418616、化合物

生成物 1

HCID 190791862-(4-Chlorobutylthio)pyridine収率 65.5%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of 25.0 g (225 mmol) of 2-mercaptopyridine and 34.5 ml (247 mmol) of triethylamine in 300 ml of ethanol, 28.5 ml (247 mmol) of 1-bromo-4-chlorobutane was added with stirring under ice-cooling, and the mixture was stirred at room temperature for 16 hours. The solvent was distilled off and the residue was dissolved in chloroform. The solution was washed with saturated aqueous sodium bicarbonate and water, and dried. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethyl acetate/hexane =1:3) to give 29.73 g of the desired compound (65.5% yield, pale yellow oil).

後処理

  1. temperaturecooling
  2. stirringthe mixture was stirred at room temperature for 16 hours
  3. distillationThe solvent was distilled off
  4. dissolutionthe residue was dissolved in chloroform
  5. washThe solution was washed with saturated aqueous sodium bicarbonate and water
  6. customdried
  7. distillationThe solvent was distilled off
  8. customthe residue was purified by column chromatography (eluent: ethyl acetate/hexane =1:3)

出典と根拠

ORDレコード
ord-e9a40193820a432da78afb9efd42f92a
出典データセット
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05246948

反応ノート

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