反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 205 °C
PROCEDURE
实验过程
A 300 mL Parr autoclave was charged with a solution of 10.52 g (40 mmols) of N,N-dimethyl-4-aminomethyl-2,6-di-t-butylphenol in 90 g of toluene, sealed and evacuated by a water aspirator, and then charged with 4.38 g (80 mmols) of 1,3-butadiene. The reaction mixture was heated to approximately 205° C. for 10 hours. A maximum pressure of 120 psig was obtained. After cooling, the reaction mixture was poured into a 500 mL separatory funnel, washed with approximately 2N HCl (1×50 mLs), water (1×50 mLs), and brine (1×50 mLs), dried over anhydrous magnesium sulfate, and concentrated in vacuo to afford 10.21 g (94% yield) of 2,4-di-t-butylspiro[5.5]undeca-1,4,8-trien-3-one as a brown solid. The brown solid was recrystallized from 80% ethanol to give the product as colorless crystals.
WORKUP
后处理
- customsealed
- customevacuated by a water aspirator
- customA maximum pressure of 120 psig was obtained
- temperatureAfter cooling
- additionthe reaction mixture was poured into a 500 mL separatory funnel
- washwashed with approximately 2N HCl (1×50 mLs), water (1×50 mLs), and brine (1×50 mLs)
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated in vacuo