HRID520756
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
Next, 20 mL of ethylenediamine was added to 2.0 g (12.4 mmol) of 2-chloro-5-chloromethylpyridine, and the mixture was stirred overnight. Following reaction completion, the reaction mixture was concentrated under reduced pressure, after which acetonitrile was added and insoluble matter were removed by filtration. The filtrate was concentrated under reduced pressure, giving 2.45 g (yield, 100%) of N-((6-chloropyridin-3-yl)methyl)ethane-1,2-diamine.
WORKUP
后处理
- customreaction completion
- concentrationthe reaction mixture was concentrated under reduced pressure
- additionafter which acetonitrile was added
- custominsoluble matter were removed by filtration
- concentrationThe filtrate was concentrated under reduced pressure