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Benzene → 6-Chloro-1-phenyl-1-hexanone

HRID 1758289
ノート
印刷プレビュー

反応式

HRID 1758289 の反応式
[Cl-].[Al+3].[Cl-].[Cl-].[Cl:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11](Cl)=[O:12].[CH:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C(Cl)(Cl)(Cl)Cl>[C:14]1([C:11]([CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][Cl:5])=[O:12])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=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 241BenzeneHCID 880146-Chlorohexanoyl chlorideHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 41827306-Chloro-1-phenyl-1-hexanone収率 34.6%

試薬・触媒・溶媒 1

HCID 5943Carbon Tetrachloride溶媒

実験手順

Aluminum chloride (16 g, 0.12 mol) is suspended in carbon tetrachloride (80 ml) and 6-chlorohexanoyl chloride (20 g, 0.12 mol) is added dropwise to the suspension with ice-cooling. After completion of addition, the mixture is stirred for 15 minutes and benzene (7.8 g, 0.1 mol) is added dropwise to the mixture with ice-cooling. After stirring with ice-cooling for 1 hour, the mixture is poured into ice-hydrochloric acid and extracted with carbon tetrachloride. The carbon tetrachloride extract is washed with water, saturated aqueous sodium bicarbonate, water and then saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The dried solution is distilled to obtain 5-chloropentyl phenyl ketone (7.3 g), b.p. 143°-150° C./0.5 mmHg.

後処理

  1. temperaturecooling
  2. additionAfter completion of addition
  3. temperaturecooling
  4. stirringAfter stirring with ice-
  5. temperaturecooling for 1 hour
  6. extractionextracted with carbon tetrachloride
  7. extractionThe carbon tetrachloride extract
  8. washis washed with water, saturated aqueous sodium bicarbonate, water
  9. dry with materialsaturated aqueous sodium chloride and dried over anhydrous magnesium sulfate
  10. distillationThe dried solution is distilled

出典と根拠

ORDレコード
ord-ebdf040837c94c138e474efa3d66b450
出典データセット
uspto-grants-1983_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04372953

反応ノート

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