HRID24975
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
The deferoxamine B base was then suspended in a mixture of ethanol (3.1 L) and water (0.46 L). Methanesulfonic acid was slowly added until the deferoxamine B base dissolved and the solution reached a pH of 3.5. Another 30 L of ethanol was added to the solution to precipitate deferoxamine B mesylate. The resulting suspension was then cooled to between −5° C. and 0° C. and maintained at reduced temperature for 24 h. The crystals were isolated by filtration, washed with ethanol and dried under vacuum to yield deferoxamine B mesylate (299 g) with a purity of 98% (w/w) as determined by HPLC analysis.
WORKUP
后处理
- dissolutiondissolved
- customto precipitate deferoxamine B mesylate
- temperatureThe resulting suspension was then cooled to between −5° C. and 0° C.
- temperaturemaintained
- customfor 24 h
- customThe crystals were isolated by filtration
- washwashed with ethanol
- customdried under vacuum