4-Hydroxybenzaldehyde → p-((Trimethylsilyl)oxy)benzaldehyde

HRID 1067054

反応式

HRID 1067054 の反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1.C(N(CC)CC)C.Cl[Si:18]([CH3:21])([CH3:20])[CH3:19].CCCCCC>ClCCl>[CH3:19][Si:18]([CH3:21])([CH3:20])[O:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[O:7])=[CH:4][CH:3]=1

参加物

6

実験手順

To a stirred solution of 122 g 4-hydroxybenzaldehyde (1.0 mol, available from Aldrich) and 111 g triethylamine (1.1 mol, available from Aldrich) in 1.0 L dichloromethane was added dropwise 108 g chlorotrimethylsilane (1.1 mol). This mixture was allowed to stand at room temperature for three days before 500 mL hexane was added. The mixture was filtered to remove triethylamine hydrochloride, and most of the solvent was removed at reduced pressure. A 200 mL portion of hexane was then added, the mixture filtered again, and solvent removed at reduced pressure to leave the desired product.

後処理

  1. additionwas added
  2. filtrationThe mixture was filtered
  3. customto remove triethylamine hydrochloride
  4. custommost of the solvent was removed at reduced pressure
  5. additionA 200 mL portion of hexane was then added
  6. filtrationthe mixture filtered again
  7. customsolvent removed at reduced pressure

出典と根拠

ORDレコード
ord-a1acf58fe71c4a9388823d348322928f
出典データセット
uspto-grants-2001_06
特許番号
US06245922B1

関連ノート

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