HRID1180097
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
PROCEDURE
实验过程
2.7 ml (42 mmoles) of methanesulphonic acid were added to a suspension de 6 g (21 mmoles) of the 3-(2-hydroxyethyl)-5-[1,2,4]triazol-1-ylmethyl-1H-indol-2-carboxylic acid in 120 ml of methanol. The mixture was left under stirring at reflux temperature for 3 hours. The solvent was evaporated to dryness under reduced pressure, the residue dissolved with 20 ml of a saturated bicarbonate solution and extracted 3 times with ethyl acetate. The combined organic phases were dried and evaporated to dryness, and the evaporated solid recrystallised from isopropyl alcohol/heptane to give 5.9 g (93%) of the title ester as a yellow crystalline solid.
WORKUP
后处理
- waitThe mixture was left
- temperatureat reflux temperature for 3 hours
- customThe solvent was evaporated to dryness under reduced pressure
- dissolutionthe residue dissolved with 20 ml of a saturated bicarbonate solution
- extractionextracted 3 times with ethyl acetate
- customThe combined organic phases were dried
- customevaporated to dryness
- customthe evaporated solid recrystallised from isopropyl alcohol/heptane