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
The ether solution of 1-bromo-2,5,8-heptadecatriyne, prepared according to the above operating procedure, is added dropwise under an inert atmosphere to a stirred solution, at 0° C., of sodium thiolate of N-ethylthioglycolamide prepared according to operating procedure b) above. The mixture obtained is stirred for 1 hour after the addition is finished. The solvents are then removed by evaporation under vacuum. The product obtained is dissolved in 100 cm3 of methylene chloride. The organic phase is washed with water, dried over magnesium sulphate, concentrated and then deposited onto a silica gel column. The expected amide is eluted with a mixture of methylene chloride and ethyl acetate (97-3). After evaporation of the eluent, 6 g of product are isolated and are recrystallized from isopropyl ether. 4 g of N-ethyl 3-thia-5,8,11-eicosatriynamide are obtained in the form of beige crystals having a melting point of 59° C.
WORKUP
后处理
- customprepared
- customThe mixture obtained
- additionafter the addition
- customThe solvents are then removed by evaporation under vacuum
- customThe product obtained
- washThe organic phase is washed with water
- dry with materialdried over magnesium sulphate
- concentrationconcentrated
- washThe expected amide is eluted with a mixture of methylene chloride and ethyl acetate (97-3)
- customAfter evaporation of the eluent, 6 g of product
- customare isolated
- customare recrystallized from isopropyl ether