HRID1749945
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
A solution of tert-butyl 4-[3-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)prop-2-ynyl]piperazine-1-carboxylate (0.0761 g, 0.196 mmol) obtained in Example B46, Step 4 in ethanol (5 mL) was added with Lindlar's catalyst (0.0700 g), and the mixture was stirred at room temperature for 15 hours under a hydrogen atmosphere. The reaction mixture was filtered through Celite, and then the filtrate was concentrated. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain tert-butyl (Z)-4-[3-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)allyl]piperazine-1-carboxylate (0.0603 g, 79%).
WORKUP
后处理
- filtrationThe reaction mixture was filtered through Celite
- concentrationthe filtrate was concentrated
- customThe resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate)