HRID1851727
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
(S)-3-methoxymethylamino-1-(2-thienyl)propan-1-ol obtained in example 2 was dissolved in 10 ml of methanol with 8 mg of Raney-nickel. The resulting solution was provided in a glass autoclave and hydrogenated at 50° C. for 12 hours. Upon completion of hydrogenation, the reaction mixture was filtered and the solvent was removed under reduced pressure to obtain the objective compound as a crystal compound (122 mg, 95% ee; purity; 90.8% by HPLC assay). The crude product was further purified by re-crystallization in toluene to give a product with optical purity as high as 100% ee.
WORKUP
后处理
- customThe resulting solution was provided in a glass autoclave and hydrogenated at 50° C. for 12 hours
- filtrationUpon completion of hydrogenation, the reaction mixture was filtered
- customthe solvent was removed under reduced pressure