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
- 0 °C
PROCEDURE
实验过程
25 g (203 mmol) of isonicotinic acid, 35.12 g (243.7 mmol) of 2,2-dimethyl-1,3-dioxolane-4,6-dione and 49.6 g (406 mmol) of 4-dimethylaminopyridine are initially charged in 300 ml of dichloromethane, and the mixture is cooled to 0° C. A 1N solution of 46.1 g (223.4 mmol) of 1,3-dicyclohexylcarbodiimide in dichloromethane is added dropwise. The mixture is stirred at room temperature for 2 hours. The precipitate formed is filtered off and washed with dichloromethane. The filtrate is concentrated under reduced pressure. The residue is dissolved in 1200 ml of ethanol, a solution of 96.6 g (507.7 mmol) of p-toluenesulfonic acid monohydrate in 300 ml of ethanol is added and the mixture is stirred under reflux for one hour. After cooling, the ethanol is removed under reduced pressure. The residue is taken up in 1000 ml of ethyl acetate and 900 ml of water and dissolved by heating. The organic phase is separated off, washed with 600 ml of saturated sodium bicarbonate solution and saturated sodium chloride solution and dried over sodium sulfate. The mixture is concentrated under reduced pressure. The crude product is filtered through a silica gel frit using dichloromethane/methanol 10:1. Since there is still product present in the aqueous phase, it is extracted with dichloromethane and the extract is dried over sodium sulfate and concentrated under reduced pressure. The crude product is filtered through a silica gel frit using dichloromethane/methanol 10:1. This gives a total of 25.9 g (42% of theory) of product.
WORKUP
后处理
- customThe precipitate formed
- filtrationis filtered off
- washwashed with dichloromethane
- concentrationThe filtrate is concentrated under reduced pressure
- dissolutionThe residue is dissolved in 1200 ml of ethanol
- stirringthe mixture is stirred
- temperatureunder reflux for one hour
- temperatureAfter cooling
- customthe ethanol is removed under reduced pressure
- dissolution900 ml of water and dissolved
- temperatureby heating
- customThe organic phase is separated off
- washwashed with 600 ml of saturated sodium bicarbonate solution and saturated sodium chloride solution
- dry with materialdried over sodium sulfate
- concentrationThe mixture is concentrated under reduced pressure
- filtrationThe crude product is filtered through a silica gel frit
- extractionis extracted with dichloromethane
- dry with materialthe extract is dried over sodium sulfate
- concentrationconcentrated under reduced pressure
- filtrationThe crude product is filtered through a silica gel frit
- customThis gives a total of 25.9 g (42% of theory) of product