反応 #833511

ord-a85e475e5a284b7cb732c9fb8d9f8aa3

反応方程式

C=CCOc1ccc(C=O)cc1OC
3-Methoxy-4-(2-propenyloxy)benzaldehyde
[Na+].[OH-]
sodium hydroxide
Cc1cc(C)cc(C)c1
mesitylene
C=CCc1cc(C=O)cc(OC)c1O
3-allyl-4-hydroxy-5-methoxybenzaldehyde

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度After cooling
  2. 2
    洗浄The aqueous phase was washed two times with diethyl ether
  3. 3
    抽出extracted with ethyl acetate
  4. 4
    その他After drying
  5. 5
    濃縮concentrating the organic phase, there
  6. 6
    その他that crystallized
  7. 7
    温度on cooling

実験手順

3-Methoxy-4-(2-propenyloxy)benzaldehyde (19.7 g, 0.100 mol) was heated under reflux in 75 ml mesitylene (1,3,5-trimethylbenzene) for 20 hours. After cooling, 250 ml 2N sodium hydroxide were added to the reaction mixture. The aqueous phase was washed two times with diethyl ether. The aqueous phase was subsequently acidified with concentrated hydrochloric acid under ice cooling and then extracted with ethyl acetate. After drying and concentrating the organic phase, there remained a light orange-colored oil that crystallized on cooling.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07393367B2uspto-grants-2008_07