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
- -60 °C
PROCEDURE
实验过程
A mixture of 7.53 g of diisopropylamine in 150 ml of anhydrous tetrahydrofuran is cooled under a stream of nitrogen to -60° C. 46.6 ml of a 1.6M solution of n-butyl-lithium in hexane is added dropwise a this temperature. When the addition is complete, the temperature of the reaction medium is allowed to rise to 5° C., the mixture is stirred for 10 minutes at this temperature and cooled to -80° C. and a solution of 10 g of 2,3-dihydro-2-benzofuranone in 150ml of anhydrous tetrahydrofuran is added dropwise. The mixture is maintained for 10 minutes at -80° C. and then for 10 minutes at -60° C. It is cooled again to -80° C. and a solution of 18.8 g of benzyl bromoacetate in 16.05 g of hexamethylphosphorotriamide is added. The temperature is allowed to rise to 20° C., and the reaction mixture is stirred for 1 hour at this temperature and hydrolyzed at 0° C. using 26 ml of saturated ammonium chloride solution. The medium is then poured into 2.5 L of 1% strength hydrochloric acid solution. The precipitate is filtered off and dissolved in 200 ml of benzene, the organic phase is washed with water and dried over anhydrous sodium sulfate and the solvent is evaporated off. The residue is recrystallized in petroleum ether.
WORKUP
后处理
- additionWhen the addition
- customto rise to 5° C.
- temperaturecooled to -80° C.
- temperatureThe mixture is maintained for 10 minutes at -80° C.
- waitfor 10 minutes at -60° C
- temperatureIt is cooled again to -80° C.
- customto rise to 20° C.
- stirringthe reaction mixture is stirred for 1 hour at this temperature and hydrolyzed at 0° C.
- filtrationThe precipitate is filtered off
- dissolutiondissolved in 200 ml of benzene
- washthe organic phase is washed with water
- dry with materialdried over anhydrous sodium sulfate
- customthe solvent is evaporated off
- customThe residue is recrystallized in petroleum ether