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
- -5 °C
PROCEDURE
实验过程
In this preparation 0.0525 mole of sodium hydride in a 50% mineral oil mixture is stirred in 300 ml. of anhydrous tetrahydrofuran, under nitrogen, then cooled to -30° C and 0.055 mole of glycidol is added dropwise. The mixture is allowed to warm to -5° C and stirred for ten minutes and then recooled to -30° C. A solution of 0.05 mole of 2-ethylsulfinyl-5-[2-(bicyclo[2.2.1]hept-7-yl)ethylaminocarbonyl]thiazole in 100 ml. of anhydrous tetrahydrofuran is added dropwise and the resulting mixture allowed to warm to 0° C. Additional solvent is added as needed to facilitate stirring. The mixture is maintained for 30 minutes at 0° C and then poured into 500 ml. of ethyl acetate, extracted with 100 ml. of water, and then with 100 ml. of aqueous saturated sodium chloride and dried over anhydrous magnesium sulfate and filtered. The filtrate is evaporated under vacuum affording an oily residue which is then further purified by chromatography on silica gel eluting with 40% ethyl acetate-60% hexane, by vol., affording 1,2-epoxy-3-(5-[2-(bicyclo[2.2.1]hept-7-yl)ethylaminocarbonyl]thiazole-2-yloxy)propane.
WORKUP
后处理
- stirringstirred for ten minutes
- customrecooled to -30° C
- temperatureto warm to 0° C
- additionAdditional solvent is added
- stirringto facilitate stirring
- temperatureThe mixture is maintained for 30 minutes at 0° C
- additionpoured into 500 ml
- extractionof ethyl acetate, extracted with 100 ml
- dry with materialof aqueous saturated sodium chloride and dried over anhydrous magnesium sulfate
- filtrationfiltered
- customThe filtrate is evaporated under vacuum
- customaffording an oily residue which
- customis then further purified by chromatography on silica gel eluting with 40% ethyl acetate-60% hexane, by vol.