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Imidazole → 1-(6-Chloro-3,4-dihydronaphthalen-1-yl)-1H-imidazole

HRID 1591075
ノート
印刷プレビュー

反応式

HRID 1591075 の反応式
S(Cl)(Cl)=O.[NH:5]1[CH:9]=[CH:8][N:7]=[CH:6]1.[Cl:10][C:11]1[CH:12]=[C:13]2[C:18](=[CH:19][CH:20]=1)[C:17](=O)[CH2:16][CH2:15][CH2:14]2.C(=O)([O-])[O-].[K+].[K+]>C(Cl)Cl.O>[Cl:10][C:11]1[CH:12]=[C:13]2[C:18](=[CH:19][CH:20]=1)[C:17]([N:5]1[CH:9]=[CH:8][N:7]=[CH:6]1)=[CH:16][CH2:15][CH2:14]2
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 795ImidazoleHCID 11430Potassium CarbonateHCID 24386Thionyl ChlorideHCID 122911496-Chloro-1-tetralone

生成物 1

HCID 233653621-(6-Chloro-3,4-dihydronaphthalen-1-yl)-1H-imidazole

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6344
Dichloromethane
溶媒

実験手順

0.218 ml of thionyl chloride is added within a period of 15 minutes to a solution of 815 mg of imidazole in 3.2 ml of methylene chloride. At the end of the exothermic reaction, 451 mg of 6-chloro-1-tetralone are added to the resulting suspension. After stirring for 20 hours at room temperature, 497 mg of potassium carbonate in 2 ml of water are added, and the mixture is extracted twice with chloroform. After drying the organic extracts over sodium sulfate, concentration is carried out under reduced pressure. The resulting crude product is purified by column chromatography (SiO2, 0.04-0.063 mesh, 0.15 bar, ethyl acetate); m.p. (after dry crystallisation from ether) 68°-72°.

後処理

  1. additionare added to the resulting suspension
  2. extractionthe mixture is extracted twice with chloroform
  3. customAfter drying the organic extracts
  4. concentrationover sodium sulfate, concentration
  5. customThe resulting crude product is purified by column chromatography (SiO2, 0.04-0.063 mesh, 0.15 bar, ethyl acetate)
  6. dry with materialm.p. (after dry crystallisation from ether) 68°-72°

出典と根拠

ORDレコード
ord-782dfac174ce446899055ac0ec25a492
出典データセット
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05206256

反応ノート

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