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 yield of 2,6-dimethyl-4-propoxyazobenzene (20.2 g) from the previous step was dissolved in 95% alcohol (175 ml). Water was added (160 ml) and the mixture was heated to reflux. Sodium hydrosulfite (Na2S2O4) (44.8 g) was added to the boiling solution in small portions. After completion of this addition, reflux was continued for 30-60 min. The alcohol was removed by distillation at reduced pressure. The remaining heterogeneous residue was made alkaline and was extracted with ether. The ether extract was dried (Na2SO4), filtered, and evaporated. The residual oil was fractionated by distillation in vacuo. After a forerun of aniline, the desired product distilled at 101° C. (0.7 mmHg); nD25 =1.5393. The yield of 2,6-dimethyl-4-propoxyaniline was 6.86 g (51%).
WORKUP
后处理
- temperaturethe mixture was heated to reflux
- additionAfter completion of this addition
- temperaturereflux
- customThe alcohol was removed by distillation at reduced pressure
- extractionwas extracted with ether
- extractionThe ether extract
- dry with materialwas dried (Na2SO4)
- filtrationfiltered
- customevaporated
- distillationThe residual oil was fractionated by distillation in vacuo
- distillationAfter a forerun of aniline, the desired product distilled at 101° C. (0.7 mmHg)