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
Ethyl 4-(4-oxobutyl)benzoate (4.63 g., 21 mmol.) is added dropwise to 1-amino-3-(tetrahydro-2H-pyran-2-yloxy)octane (4.82 g., 21 mmol.) at ambient temperature. The resulting mixture is stirred for 15 minutes before adding anhydrous sodium sulfate (4 g.), and then stirred for 1 hour. The solid is subsequently removed by filtration and washed with a small quantity of benzene. The combined filtrate and washings are diluted with benzene (70 ml.) and then treated with mercaptoacetic acid (1.93 g., 21 mmol.). The resulting solution is refluxed in a Dean-Stark apparatus for 3 hours. The reaction mixture is allowed to cool to room temperature, washed successively with dilute hydrochloric acid, 5% sodium bicarbonate, dried over anhydrous magnesium sulfate, and concentrated to give an oil residue. A methanol solution (50 ml.) of the oil residue is treated with concentrated hydrochloric acid (0.2 ml.) and then stirred at ambient temperature for 16 hours. The reaction mixture is diluted with cold water, followed by extraction with ether. The ethereal extract is washed with water, 5% sodium bicarbonate, dried over anhydrous magnesium sulfate, and filtered. Evaporation of the filtrate in vacuo provides an oil residue which is then applied to a silica gel column (300 g.) with chloroform. Elution with chloroform-methanol (100:1; v:v; 1950 ml.) provides impure material; further elution with the same eluant (450 ml.) gives the title compound as a pale yellow oil (2.80 g., 6.64 mmol., 31%), pmr (CDCl3) δ0.90 (3H, t), 1.40 (3H, t), 3.53 (2H, s), 4.40 (2H, q), 4.70 (1H, m), 7.22 (2H, d), 8.0 (2H, d).
WORKUP
后处理
- stirringstirred for 1 hour
- customThe solid is subsequently removed by filtration
- washwashed with a small quantity of benzene
- additionThe combined filtrate and washings are diluted with benzene (70 ml.)
- temperatureThe resulting solution is refluxed in a Dean-Stark apparatus for 3 hours
- washwashed successively with dilute hydrochloric acid, 5% sodium bicarbonate
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated
- customto give an oil residue
- stirringstirred at ambient temperature for 16 hours
- extractionfollowed by extraction with ether
- extractionThe ethereal extract
- washis washed with water, 5% sodium bicarbonate
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- customEvaporation of the filtrate in vacuo
- customprovides an oil residue which
- washElution with chloroform-methanol (100:1; v:v; 1950 ml.)
- customprovides impure material
- washfurther elution with the same eluant (450 ml.)