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
Oven dried glassware and a nitrogen purge were utilized. 3.22 mL of 1.6 Molar n-butyl lithium in hexanes (5.15 mmol) was added dropwise to a solution of 1.06 g (4.93 mmol) of 6-ethyl-5-methyl-2-phenyl-5,6-dihydropyrimidin-4-one, in 15 mL of dry tetrahydrofuran, at -50 to -60° C. The mixture was stirred for 15 minutes and then 0.8 mL (5.38 mmol) of 80 wt.% propargyl bromide in toluene was added at -65° C. The ice bath was removed after 1.5 hours and the reaction mixture was stirred for an additional 20 hours. The solvent had evaporated overnight. Ether was added and the reaction mixture was washed three times with water followed by three times with 3 Molar hydrochloric acid. The acidic aqueous washes were combined, cooled externally, and 50% sodium hydroxide was added until the pH=10, then extracted three times with ether. The ether extracts were combined, dried over magnesium sulfate, and concentrated to yield 0.68 g of crude product. The crude product was combined with crude product obtained from previous reactions and purified on a six inch plug of basic alumina by washing with 400 mL of methylene chloride. The filtrate was concentrated to yield 6-ethyl-5-methyl-2-phenyl-3-propargyl-5,6-dihydropyrimidin-4-one (Compound 1), as a yellow solid, melting 62°-65° C.
WORKUP
后处理
- customOven dried glassware
- customa nitrogen purge
- customThe ice bath was removed after 1.5 hours
- stirringthe reaction mixture was stirred for an additional 20 hours
- customThe solvent had evaporated overnight
- additionEther was added
- washthe reaction mixture was washed three times with water
- temperaturecooled externally
- addition50% sodium hydroxide was added until the pH=10
- extractionextracted three times with ether
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- customto yield 0.68 g of crude product
- customobtained from previous reactions
- custompurified on a six inch plug of basic alumina
- washby washing with 400 mL of methylene chloride
- concentrationThe filtrate was concentrated