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
To a 1 L Erlenmeyer flask was added 2-triphenylenecarbaldehyde 5.13 g, (20 mmol), 2-methyl-2-amino-1,3-propanediol (Aldrich, 2.2 g, 21 mmol), p-toluenesulfonic acid.H2O (Eastman Kodak Co., Rochester, NY, 14650, 0.1 g, 0.5 mmol), and PhCH3 (250 mL). The mixture was warmed to reflux for a few minutes and H2O (2-3 mL) was driven off. The resulting golden colored solution was allowed to cool to RT, diluted with absolute EtOH (250 mL) and stirred overnight. NaBH3CN (Aldrich, 95%, 0.63 g, 10 mmol) was added to the reaction. After the NaBH3CN dissolved, an indicator (bromocresol green, Eastman, 5 mg) was added. To the resulting blue solution was added 5 drops of 1M solution of HCl gas in absolute EtOH every 15 minutes. After 3 days the indicator turned green then yellow and voluminous white precipitate was present in the flask. To the flask was then added 1M gas HCl (10 mL) in absolute EtOH. The reaction was diluted to 2 L with absolute ether and stirred for 1 h. The precipitate was then collected by filtration through a medium porosity glass fritted funnel and pressed dry. The filter cake was washed thoroughly with 20% HCL (2×250 mL), pressed dry and then washed with CH2Cl2 (4×500 mL), pressed and sucked dry. The crude off-white solid was then recrystallized (EtOH/Et2O) 3× to give after drying (100°) 3.34 g (43%) of 2-methyl-2-((2-triphenylenylmethyl)amino)-1,3-propanediol hydrochloride.1/2H2O mp 207°-208.5° (dec), (C, H, Cl, N).
WORKUP
后处理
- temperatureThe mixture was warmed
- temperatureto reflux for a few minutes
- waitAfter 3 days the indicator turned green
- stirringstirred for 1 h
- filtrationThe precipitate was then collected by filtration through a medium porosity glass fritted funnel
- custompressed dry
- washThe filter cake was washed thoroughly with 20% HCL (2×250 mL)
- custompressed dry
- washwashed with CH2Cl2 (4×500 mL)
- customsucked dry
- customThe crude off-white solid was then recrystallized (EtOH/Et2O) 3×
- customto give
- dry with materialafter drying (100°) 3.34 g (43%) of 2-methyl-2-((2-triphenylenylmethyl)amino)-1,3-propanediol hydrochloride