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p-Bromoacetophenone → 4-Bromo-1-(1,3-dithian-2-yl)ethylbenzene

HRID 55628
ノート
印刷プレビュー

反応式

HRID 55628 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[CH3:9])=[CH:4][CH:3]=1.[CH2:11]([SH:15])[CH2:12][CH2:13][SH:14].B(F)(F)F.[CH3:20]COCC>ClC(Cl)Cl.ClCCl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH:9]2[S:15][CH2:11][CH2:12][CH2:13][S:14]2)[CH3:20])=[CH:4][CH: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

6

反応物 3

HCID 7466p-BromoacetophenoneHCID 8000Boron trifluoride etherateHCID 80131,3-Propanedithiol

生成物 1

HCID 219601124-Bromo-1-(1,3-dithian-2-yl)ethylbenzene

試薬・触媒・溶媒 2

HCID 6212Chloroform溶媒HCID 6344Dichloromethane溶媒

実験手順

To the compound p-bromoacetophenone (36.85 g, 185 mmol) in trichloromethane (300 ml) was added 1,3-propanedithiol (25 g, 230 mmol) and boron trifluoride etherate (3 ml). The resulting mixture was stirred at room temperature for 48 hours. The mixture was diluted with dichloromethane (500 ml), washed twice with 10% sodium hydroxide (200 ml), water, and brine, and then dried (Na2SO4). The product was concentrated to an oil. A portion was stirred with ether (100 ml) and a crystalline product was formed. The crystalline product was recovered by filtration and purified by recrystallization to yield 4-bromo-1-(1,3-dithian-2-yl)ethylbenzene.

後処理

  1. washwashed twice with 10% sodium hydroxide (200 ml), water, and brine
  2. dry with materialdried (Na2SO4)
  3. concentrationThe product was concentrated to an oil
  4. stirringA portion was stirred with ether (100 ml)
  5. customa crystalline product was formed
  6. filtrationThe crystalline product was recovered by filtration
  7. custompurified by recrystallization

出典と根拠

ORDレコード
ord-6cb87811cba8461b8d090235ec7639ac
出典データセット
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05624927

反応ノート

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