Реакция #2389080
ord-8201d360a54a443daad22402d726eea2
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ПромывкаThe hydrogenator is washed with nitrogen in order
- 2workup.ADDITIONhydrogen is introduced at the pressure of 2.5 atmospheres
- 3ДругоеFor a period of time of 9 hours the temperature of reaction
- 4Другоеis kept at 50° C.
- 5Промывкаthe hydrogenator is washed with nitrogen
- 6Фильтрацияthe reaction mixture is filtered in order
- 7КонцентрированиеThe solution is concentrated to 130 ml
- 8workup.ADDITIONdiluted with 45 ml of water
- 9workup.ADDITIONadded with 18.2 g of sodium metabisulfite
- 10Температураis cooled to 0° C
- 11ДругоеThe so obtained suspension
- 12workup.WAITis kept at 0° C. for two hours
- 13Фильтрацияis filtered
- 14Промывкаthe solid is washed with 60 ml of isopropanol
- 15Температураcooled to 0° C.
- 16Температураhalf at room temperature, then is heated at 60° C.
- 17Другоеthe layers are separated
- 18ПромывкаThe organic phase is washed with 60 ml of water
- 19Концентрированиеis concentrated under vacuum at 60° C. until an oil
- 20Другоеis obtained which
- 21Температураby cooling
- 22Температураthe resulting solution is cooled to 0° C. in two hours
- 23workup.WAITThe obtained suspension is kept for one hour at this temperature
- 24Фильтрацияfiltered
- 25Промывкаwashed with 10 ml of cold isopropanol
- 26Другоеdried in oven under vacuum until constant weight
Методика
49.44 Grams (0.154 moles) of 4-(5-bromo-6-methoxy-2-naphthyl)-4-hydroxybut-3-en-2-one, 12.24 g (0.149 moles) of anhydrous sodium acetate, 4 g of a 50% suspension in water of 5% palladium on carbon, equivalent to 0.00094 moles of palladium and 400 ml of isopropanol are put into a hydrogenator. The hydrogenator is washed with nitrogen in order to eliminate the oxygen and then hydrogen is introduced at the pressure of 2.5 atmospheres. For a period of time of 9 hours the temperature of reaction is kept at 50° C., then the hydrogen is let off, the hydrogenator is washed with nitrogen and the reaction mixture is filtered in order to eliminate the catalyst. The solution is concentrated to 130 ml, diluted with 45 ml of water, heated to 60° C. and added with 18.2 g of sodium metabisulfite. The reaction mixture is kept for one hour at 60° C. and then is cooled to 0° C. The so obtained suspension is kept at 0° C. for two hours and then is filtered; the solid is washed with 60 ml of isopropanol cooled to 0° C. and then is suspended in a mixture made by 70 ml of a 10% aqueous solution of sodium hydroxide and 270 ml of toluene. The reaction mixture is stirred for one hour and half at room temperature, then is heated at 60° C. and the layers are separated. The organic phase is washed with 60 ml of water and is concentrated under vacuum at 60° C. until an oil is obtained which solidifies by cooling. The solid is dissolved at 60° C. in 40 ml of isopropanol and the resulting solution is cooled to 0° C. in two hours. The obtained suspension is kept for one hour at this temperature, filtered, washed with 10 ml of cold isopropanol and dried in oven under vacuum until constant weight. 26.3 Grams of nabumetone are obtained with a yield equal to 74.8%.