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
12.5 g of 1-phenyl-1,2-propanedione-2-oxime and 10 ml of p-tolualdehyde are added to 50 ml of glacial acetic acid, and HCl gas is introduced for 30 minutes, with ice-cooling. The product is precipitated as the hydrochloride by addition of methyl tert-butyl ether and filtered off with suction, and the precipitate is washed with methyl tert-butyl ether. The precipitate is suspended in water and the pH is made alkaline using ammonia. The mixture is extracted three times with in each case 200 ml of dichloromethane, the combined organic phases are dried over MgSO4 and the solvent is then removed under reduced pressure. This gives 6.4 g of 4-methyl-5-phenyl-2-p-tolyloxazole 3-oxide as a white solid. C17H15NO2 (265.31), MS (ESI)=266 (M+H+).
WORKUP
后处理
- additionis introduced for 30 minutes, with ice-
- temperaturecooling
- customThe product is precipitated as the hydrochloride by addition of methyl tert-butyl ether
- filtrationfiltered off with suction
- washthe precipitate is washed with methyl tert-butyl ether
- extractionThe mixture is extracted three times with in each case 200 ml of dichloromethane
- dry with materialthe combined organic phases are dried over MgSO4
- customthe solvent is then removed under reduced pressure