反応 #1745

ord-9d8b4bad4cfc4f6f9993dde1eca90539

反応方程式

OC1CCC(c2ccccc2)CC1
4-phenylcyclohexanol
CC(=O)OC(C)=O
acetanhydride
CC(=O)OC1CCC(c2ccccc2)CC1
O-acetyl-4-phenylcyclohexanol
収率 92.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONare added
  2. 2
    温度This is heated to 80° C. for 3 hours
  3. 3
    その他The crystalline product precipitated
  4. 4
    ろ過filtered
  5. 5
    workup.DISSOLUTIONdissolved in ether
  6. 6
    洗浄washed with sodium bicarbonate solution
  7. 7
    その他dried
  8. 8
    その他evaporated down in vacuo

実験手順

To a mixture of 20.3 g (0.115 mol) of 4-phenylcyclohexanol, 14.2 ml (0.15 mol) of acetanhydride and 29 ml of triethylamine are added, with stirring and at ambient temperature, 2.3 g (0.02 mol) of 4-dimethylaminopyridine, a clear solution being produced in an exothermic reaction. This is heated to 80° C. for 3 hours and the reaction mixture is then poured into ice water. The crystalline product precipitated is suction filtered, dissolved in ether, washed with sodium bicarbonate solution, dried and evaporated down in vacuo. 23 g (92% of theory) of O-acetyl-4-phenylcyclohexanol are obtained. The product is obtained initially as an oil but crystallises when left to stand.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05726205uspto-grants-1998_03