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
CONDITIONS
反应条件
- 温度
- 80 °C
PROCEDURE
实验过程
A mixture of (1-methyl-5-oxopyrrolidin-2-yl)methyl 4-methylbenzenesulfonate (196 g, 0.73 mol), sodium azide (142 g, 2.19 mol) and N-methyl-2-pyrrolidinone (800 ml) was heated to 80° C. for two hours, cooled, diluted with diethyl ether (3 L) and filtered through a pad of silica gel. The silica gel pad was washed with 1 L of a mixture of methanol:diethyl ether (5:1). The combined filtrates were concentrated in vacuo. The residue was subsequently treated with a suspension of sodium hydride in mineral oil (60%, 44 g, 1.1 mol) at 10-15° C. under rapid stirring for two hours followed by the addition of lithium iodide (155 g, 1.1 mol). The reaction mixture was allowed to warm to 25° C. for 3 hours. The unreacted sodium hydride was quenched with water. The mixture was diluted with dioxane (1.5 L) and diethyl ether (5 L) and filtered through a plug of silica gel. The silica gel plug was then washed with ether. The combined filtrates were concentrated, the residue was dissolved in dioxane (2 L), cooled to 0° C., and triphenylphosphine (191 g, 0.73 mol) was added at 0° C. for 1 hour. The reaction mixture was stirred at 25° C. for 10 hours, then water (25 mL) and aqueous ammonia (1 mL, 25%) were added, and the mixture was refluxed for two hours, cooled, and evaporated. The residue was dissolved in isopropanol (2.5 L), and to the solution was added a solution of oxalic acid (88 g, 0.7 mol) in isopropanol (1 L). The precipitate that formed was filtered, washed with isopropanol (1 L), and dried to give the title compound as the oxalate salt.
WORKUP
后处理
- temperaturecooled
- filtrationfiltered through a pad of silica gel
- washThe silica gel pad was washed with 1 L of a mixture of methanol:diethyl ether (5:1)
- concentrationThe combined filtrates were concentrated in vacuo
- temperatureto warm to 25° C. for 3 hours
- customThe unreacted sodium hydride was quenched with water
- additionThe mixture was diluted with dioxane (1.5 L) and diethyl ether (5 L)
- filtrationfiltered through a plug of silica gel
- washThe silica gel plug was then washed with ether
- concentrationThe combined filtrates were concentrated
- dissolutionthe residue was dissolved in dioxane (2 L)
- temperaturecooled to 0° C.
- stirringThe reaction mixture was stirred at 25° C. for 10 hours
- temperaturethe mixture was refluxed for two hours
- temperaturecooled
- customevaporated
- dissolutionThe residue was dissolved in isopropanol (2.5 L)
- customThe precipitate that formed
- filtrationwas filtered
- washwashed with isopropanol (1 L)
- customdried