反応 #346977

ord-87cd6f1e92bf4f9db1d60da7612057ac

反応方程式

CC(C)(C)[O-].[K+]
potassium tertiary butoxide
C=Cc1ccc(OC(C)=O)cc1
p-acetoxystyrene
C=Cc1ccc([O-])cc1.[K+]
potassium p-vinylphenolate

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONDuring this addition
  2. 2
    温度the reaction solution was maintained at a temperature below 20° C
  3. 3
    workup.ADDITIONAt the end of addition

実験手順

With ice cooling, 310 ml of a 1.0-M solution of potassium tertiary butoxide in tetrahydrofuran was stirred until a temperature of 5° C. was reached. To the solution, 50 grams (0.31 mol) of p-acetoxystyrene was added dropwise over 30 minutes. During this addition, the reaction solution was maintained at a temperature below 20° C. At the end of addition, the solution was allowed to stand under the conditions for 30 minutes, obtaining a yellowish orange colored tetrahydrofuran solution of potassium p-vinylphenolate. With stirring and ice water cooling, a solution of 67.28 grams (0.31 mol) of di-t-butyl dicarbonate in 60 ml of tetrahydrofuran was added dropwise to the reaction solution, which was maintained at a temperature below 20° C. At the end of addition, the reaction mixture was stirred for one hour at room temperature. It was combined with 30 ml of saturated saline water and shaken for subsequent decantation. The organic layer was dried over anhydrous sodium sulfate and the solvent distilled off. The oily residue was subjected to vacuum distillation, yielding 65 grams of a colorless oily product as a fraction of 90° to 92° C. /0.2 mmHg. It was p-t-butoxy-carbonyloxystyrene (GC 98.5%, yield 95.7%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05523370uspto-grants-1996_06