Sesamol → Ethanone, 1-(6-hydroxy-1,3-benzodioxol-5-yl)-

HRID 1749916ノート

反応式

HRID 1749916 の反応式
[CH2:1]1[O:5][C:4]2[CH:6]=[C:7]([OH:10])[CH:8]=[CH:9][C:3]=2[O:2]1.[C:11]([O-])(=[O:13])[CH3:12].[Na+]>C(OC(=O)C)(=O)C>[OH:10][C:7]1[C:8]([C:11](=[O:13])[CH3:12])=[CH:9][C:3]2[O:2][CH2:1][O:5][C:4]=2[CH:6]=1

参加物

4

反応条件

温度
90 °C

実験手順

A solution of sesamol (5.6 g, 40 mmol) in acetic anhydride (20 mL) was cooled to 0° C. under an argon atmosphere. The solution was slowly added with boron trifluoride/diethyl ether complex (10 mL), and then the mixture was stirred at 90° C. for 2 hours. The reaction mixture was added to saturated aqueous sodium acetate (50 mL), and the mixture was stirred at room temperature. The solid formed was removed by filtration, and then the reaction mixture was extracted with ethyl acetate, and the organic layer was successively washed with saturated aqueous sodium hydrogencarbonate, water and saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residual solid was suspended in methanol, thereby washed, then collected by filtration and dried to obtain 1-(6-hydroxybenzo[d][1,3]dioxol-5-yl)ethanone (5.9 g, 82%).

後処理

  1. additionThe solution was slowly added with boron trifluoride/diethyl ether complex (10 mL)
  2. stirringthe mixture was stirred at room temperature
  3. customThe solid formed
  4. customwas removed by filtration
  5. extractionthe reaction mixture was extracted with ethyl acetate
  6. washthe organic layer was successively washed with saturated aqueous sodium hydrogencarbonate, water and saturated brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customThe solvent was evaporated under reduced pressure
  9. washwashed
  10. filtrationcollected by filtration
  11. customdried

出典と根拠

ORDレコード
ord-b1059b7d76534a23955b2b957c8ce9b2
出典データセット
uspto-grants-2015_10
特許番号
US09156827B2

反応ノート

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