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 hydrazone (20 g.) was then refluxed for 3 hours with a solution containing water (200 ml.), ethanol (40 ml.), benzaldehyde (25 ml.) and benzoic acid (2.5 g.). The solution was cooled and then decanted from benzaldehyde phenylhydrazone, extracted three times with chloroform, decolorized with carbon and concentrated at reduced pressure. The resulting syrup was further evaporated with several portions of absolute ethanol to remove residual water and the resulting syrup (10 g.) was left to crystallize. The crystals were filtered with ethanol to give α-L-mannopyranose, m.p. 125°-126°, [α]D -26.9°→-14.4° (24 hr., c 2.0, water) compared to m.p. 128°-132°, [α]D -14.5° (equilibrium, c 3.4, water).
WORKUP
后处理
- temperatureThe solution was cooled
- customdecanted from benzaldehyde phenylhydrazone
- extractionextracted three times with chloroform
- concentrationconcentrated at reduced pressure
- customThe resulting syrup was further evaporated with several portions of absolute ethanol
- customto remove residual water
- waitthe resulting syrup (10 g.) was left
- customto crystallize
- filtrationThe crystals were filtered with ethanol