Water → 1-Bromo-4-(4-chlorostyryl)benzene

HRID 549477ノート

反応式

HRID 549477 の反応式
[Br-].[Br:2][C:3]1[CH:28]=[CH:27][C:6]([CH2:7][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=[CH:5][CH:4]=1.[H-].[Na+].[Cl:31][C:32]1[CH:39]=[CH:38][C:35]([CH:36]=O)=[CH:34][CH:33]=1.O>CN(C=O)C.CCOCC>[Br:2][C:3]1[CH:4]=[CH:5][C:6]([CH:7]=[CH:36][C:35]2[CH:38]=[CH:39][C:32]([Cl:31])=[CH:33][CH:34]=2)=[CH:27][CH:28]=1

参加物

7

反応条件

温度
0 °C

実験手順

To a solution of (4-bromobenzyl)triphenylphosphonium bromide (396 g; 0.77 mol) in 2.5 L of DMF at 0° C., was added 37 g (0.92 mol) of NaH (60% in oil) in four portions. The solution was stirred 1 hr at 0° C. followed by the addition of 109 g (0.77 mol) of 4-chlorobenzaldehyde in two portions. This mixture was warmed up to room temperature, stirred 1 hr and quench by pouring the reaction into a 5° C. mixture of 10 L of water and 2.5 L of Et2O. Aqueous layer was extracted with Et2O, combined organic layers were washed with brine and dried over Na2SO4. Volatiles were removed under reduced pressure and the residue was dissolved in 1.5 L of cyclohexane and filtered through a pad of silica gel (wash with cyclohexane). 16 g of one isomer cristallized out of the solution as a white solid and after evaporation of the volatiles, 166 g of the other isomer 1-bromo-4-[2-(4-chlorophenyl)vinyl]benzene was isolated.

後処理

  1. temperatureThis mixture was warmed up to room temperature
  2. stirringstirred 1 hr
  3. customquench
  4. additionby pouring
  5. customthe reaction into a 5° C.
  6. extractionAqueous layer was extracted with Et2O
  7. washwere washed with brine
  8. dry with materialdried over Na2SO4
  9. customVolatiles were removed under reduced pressure
  10. dissolutionthe residue was dissolved in 1.5 L of cyclohexane
  11. filtrationfiltered through a pad of silica gel (wash with cyclohexane)
  12. customafter evaporation of the volatiles

出典と根拠

ORDレコード
ord-154acbd594c045ba8dc50af4335bb37a
出典データセット
uspto-grants-2011_05
特許番号
US07943649B2

反応ノート

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