HRID2307446
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 solution of (S)-{1-[3-(2-methyl-morpholin-4-yl)-phenyl]-ethyl}-carbamic acid tert-butyl ester (2.62 g, 8.19 mmol), and hydrochloric acid (1.0M solution in diethyl ether) (12.3 ml, 3eq) in methanol (25 ml) was stirred at room temperature overnight. Concentrated under vacuum and 2.43 g of hydrochloric acid salt of (S)-1-[3-(2-methyl-morpholin-4-yl)-phenyl]-ethylamine was obtained as yellow solid (quantitative yield).
WORKUP
后处理
- concentrationConcentrated under vacuum and 2.43 g of hydrochloric acid salt of (S)-1-[3-(2-methyl-morpholin-4-yl)-phenyl]-ethylamine