تفاعل #2025293
ord-a5a409c04ed542e3a58f8a2daf4c7b5e
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىAfter completion of the reaction
- 2ترشيحthe precipitates were filtered off
- 3workup.ADDITION200 ml of toluene were added
- 4غسيلby washing with water, 5% acetic acid, water, 5% aqueous sodium hydrogen carbonate solution and water in this order
- 5تجفيفAfter the organic phase was dried over anhydrous magnesium sulfate
- 6workup.DISTILLATIONthe solvent was distilled off under reduced pressure
- 7أخرىThe resulting residue was purified by silica gel column chromatography (eluent; toluene:ethyl acetate)
الإجراء التجريبي
Into 20 ml of dichloromethane were dissolved 1.78 g (5 millimoles) of the (+)-2-{4-(1-hydroxyethyl)phenyl}-5-decyloxypyrimidine obtained in Preparation Example [starting material compound (VI)] 70 and 1.2 g (6 millimoles) of dodecanic acid, and then 1.4 g of N,N'-dicyclohexylcarbodiimide and 0.1 g of 4-pyrrolidinopyridine were added thereto, followed by stirring at room temperature for 24 hours. After completion of the reaction, the precipitates were filtered off and 200 ml of toluene were added thereto, followed by washing with water, 5% acetic acid, water, 5% aqueous sodium hydrogen carbonate solution and water in this order. After the organic phase was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent; toluene:ethyl acetate) to obtain 2.53 g (yield: 94%) of (+)-2-{4-(1-dodecanoyloxyethyl)phenyl}-5-decyloxypyrimidine. The physical values are shown in Table-1.