别名：n-boc-3,4-环氧哌啶
英文名称：1-boc-3,4-epoxypiperidine
分子式：c10h17no3
cas no.：161157-50-2
分子量：199.25
结构式：
规格：95%
用途：基础原料、有机中间体、医药中间体
合成工艺如下：
sodium hydrogencarbonate; dichloromethane; water;
reactants are commercially availlable.
fujisawa pharmaceutical co., ltd., us6355640, b1, (2002) to a solution of 1-tert-butoxycarbonyl-1,2,3,6-tetrahydropyridine (18.9 g) in dichloromethane (400 ml).. was added in turn sodium hydrogen carbonate (11.3 g) and m-chloroperoxybenzoic acid (23.4 g) wi th care at 0°c., and which was stirred for 2 hours.. insoluble material was removed by filtration, mother liquor was washed saturated sodium chloride in water (100 ml) and dried over magnesium sulfat e.. evaporation of the solvent gave a residue, which was dissolved in n-hexane (300 ml) and insoluble material was removed by filtration.. mother liquor was concentrated in vacuo, the remainings were dissolved in ethyl acetate (300 ml) and washed in turn with saturated sodium hydrogen carbonate in water (100 ml*5) and saturated sodium chloride in water (100 ml*2), which was dried over magnesium su lfate.. evaporation of the solvent gave a residue, which was chromatographed on silica gel (350 ml) eluding in turn with 10percent, 20percent and 30percent ethyl acetate in n-hexane.. tractions, conta ining desired product, were collected and concentrated in vacuo to give 1-tert-butoxycarbonyl-3,4-epoxypiperidine (13.7 g). nmr (cdcl3, delta): 1.45 (9h, s), 1.75-2.10 (2h, m), 3.00-4.00 (6h, m).