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
In a 100 mL three-necked round-bottomed flask fitted with a mechanical stirrer, nitrogen inlet and thermometer was placed 0.62 g (3 mmol) of 4-amino-3,5-dichlorobenzoic acid, 20 mL of tetrahydrofuran, and 1.52 g (15 mmol) of triethylamine. To the resulting well-stirred mixture was added 0.4 g (3.3 mmol) of methanesulfonyl chloride dropwise while keeping the reaction temperature at -25° C. The resulting suspension was stirred at -25° C. for 30 minutes, after which 0.7 g (3.8 mmol) of 3-amino-1-chloro-3-methyl-2-pentanone hydrochloride was added slowly over a 45 minute period. After the addition was complete, the reaction mixture was stirred at -25° C. for an additional 60 minutes. The cooling bath was removed; the reaction mixture was allowed to warm to room temperature and stirred for 3 hours. The reaction mixture was poured into a mixture of water and ethyl acetate. The phases were separated and the aqueous layer was extracted several times with ethyl acetate. The combined organic phases were washed sequentially with water, saturated aqueous sodium bicarbonate, and water, then dried over anhydrous magnesium sulfate. The resulting solution was treated with charcoal and filtered through Celite™. The solvent was removed using a rotary evaporator, yielding 0.84 g of 4-amino-3,5-dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl) benzamide as a white solid, mp 134°-138° C.
WORKUP
后处理
- customIn a 100 mL three-necked round-bottomed flask fitted with a mechanical stirrer, nitrogen inlet
- customat -25° C
- stirringThe resulting suspension was stirred at -25° C. for 30 minutes
- additionAfter the addition
- stirringthe reaction mixture was stirred at -25° C. for an additional 60 minutes
- customThe cooling bath was removed
- stirringstirred for 3 hours
- additionThe reaction mixture was poured into a mixture of water and ethyl acetate
- customThe phases were separated
- extractionthe aqueous layer was extracted several times with ethyl acetate
- washThe combined organic phases were washed sequentially with water, saturated aqueous sodium bicarbonate, and water
- dry with materialdried over anhydrous magnesium sulfate
- additionThe resulting solution was treated with charcoal
- filtrationfiltered through Celite™
- customThe solvent was removed
- customa rotary evaporator