反応 #66942

ord-f526c903b5bf482daf69f8cfb513b16b

反応方程式

O=Cc1ccc(O)cc1
4-Hydroxybenzaldehyde
CC(C)=O
acetone
CC(=O)C=Cc1ccc(O)cc1
pale yellow solid
収率 70.4%
CC(=O)C=Cc1ccc(O)cc1
4-(4-Hydroxyphenyl)-3-buten-2-one
収率 70.4%

試薬

なし

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe reaction mixture was stirred for 6 hr at room temperature
  2. 2
    その他separated solid
  3. 3
    workup.ADDITIONdiluted with water until all separated solid
  4. 4
    workup.DISSOLUTIONdissolved
  5. 5
    ろ過The precipitated solid was collected by filtration
  6. 6
    洗浄washed with water and ethanol successively
  7. 7
    その他The crude product was recrystallized from ethanol

実験手順

4-Hydroxybenzaldehyde (10 g, 82 mmol) was dissolved in 28 ml of 10% sodium hydroxide aqueous solution, then acetone (20 ml) and 10% sodium hydroxide aqueous solution (40 ml) was added under stirring, and the reaction mixture was stirred for 6 hr at room temperature. separated solid diluted with water until all separated solid dissolved. The reaction mixture was neutralized with hydrochloric acid to pH=7.0. The precipitated solid was collected by filtration and washed with water and ethanol successively. The crude product was recrystallized from ethanol to give 9.3 g of a pale yellow solid, mp: 104-105° C., yield: 70.4%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08524744B2uspto-grants-2013_09