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
To a solution of 2-(4-methylphenyl)-6,7-dihydro-5H-benzocycloheptene-8-carboxylic acid (35.0 g, 0.126 mol) in tetrahydrofuran (THF) (280 ml) were added (COCl)2 (21.9 ml, 0.251 mol) and DMF (0.7 ml) at 0° C. Under nitrogen atmosphere, the mixture was stirred at room temperature for 4 hours. After the reaction completed, The solvent was evaporated, and to the residue was added THF (315 ml). To a solution of the acid chloride was added a solution of 4-(2-tetrahydropyranyloxymethyl)aniline (28.1 g, 0.138 mol) and triethylamine (Et3N) (26.3 ml, 0.189 mol) in THF (105 ml) at 0° C., and the mixture was stirred under nitrogen atmosphere, at room temperature for 2 hours. After the reaction completed, to the mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated NaCl solution and dried with MgSO4. The solvent was evaporated and the residue was dissolved in methanol (MeOH) (470 ml). To the mixture was dropwise added 6N HCl (5.9 ml) at room temperature, and the mixture was stirred for 1 hour. After the reaction completed, the mixture was neutralized with saturated NaHCO3solution, and the solvent was removed. The residue was washed with water and then acetone/isopropylether (10:1; 60 ml), and the resulting precipitate was filtered, which was dissolved in THF. The mixture was dried with MgSO4, and the solvent was evaporated. The resulting powder was washed twice with hexane:ethyl acetate (10:1; 50 ml) to give N-(4-hydroxymethylphenyl)-2-(4-methylphenyl)-6,7-dihydro-5H-benzocycloheptene-8-carboxamide (26.8 g, 56%) as white powder.
WORKUP
后处理
- customThe solvent was evaporated
- additionto the residue was added THF (315 ml)
- stirringthe mixture was stirred under nitrogen atmosphere, at room temperature for 2 hours
- extractionthe mixture was extracted with ethyl acetate
- washThe organic layer was washed with saturated NaCl solution
- dry with materialdried with MgSO4
- customThe solvent was evaporated
- dissolutionthe residue was dissolved in methanol (MeOH) (470 ml)
- customat room temperature
- stirringthe mixture was stirred for 1 hour
- customthe solvent was removed
- washThe residue was washed with water
- filtrationacetone/isopropylether (10:1; 60 ml), and the resulting precipitate was filtered
- dissolutionwhich was dissolved in THF
- dry with materialThe mixture was dried with MgSO4
- customthe solvent was evaporated
- washThe resulting powder was washed twice with hexane:ethyl acetate (10:1; 50 ml)