Реакция #1448
ord-d699a2fd0bfb49f2b2d9d51a6a3e6ab2
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.STIRRINGagain stirred for 16 hours at room temperature
- 2Другоеthe resulting organic layer was separated
- 3Промывкаwashed with a saturated sodium chloride aqueous solution
- 4Сушкаdried over anhydrous magnesium sulfate
- 5ДругоеAfter removing the solvent
- 6workup.DISTILLATIONby distillation under a reduced pressure
- 7workup.ADDITIONthe resulting hexane eluate was mixed with 45 ml of sulfuric acid
- 8workup.WAITsubjected to 24 hours
- 9Температураof heating
- 10Температураunder reflux
- 11ТемператураAfter cooling down to room temperature
- 12workup.ADDITIONthe reaction solution was mixed with ice water and ethyl acetate
- 13Другоеto separate water layer which
- 14workup.ADDITIONwas subsequently mixed with concentrated hydrochloric acid and ethyl acetate
- 15Другоеthe resulting organic layer was separated
- 16Промывкаwashed with water
- 17Сушкаa saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate
- 18ДругоеBy removing the solvent
- 19workup.DISTILLATIONby distillation under a reduced pressure
Методика
In a stream of argon, 60% sodium hydride was dissolved in 10 ml of tetrahydrofuran, and the solution was mixed with 2.0 g of benzyl cyanide, stirred for 1 hour at room temperature, further mixed with 3.69 g of 1,4-dibromobutane and again stirred for 16 hours at room temperature. The reaction mixture was mixed with water and ethyl acetate, and the resulting organic layer was separated, washed with a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. After removing the solvent by distillation under a reduced pressure, the thus obtained residue was subjected to silica gel column chromatography, and the resulting hexane eluate was mixed with 45 ml of sulfuric acid and subjected to 24 hours of heating under reflux. After cooling down to room temperature, the reaction solution was mixed with ice water and ethyl acetate to separate water layer which was subsequently mixed with concentrated hydrochloric acid and ethyl acetate, and the resulting organic layer was separated, washed with water and a saturated sodium chloride aqueous solution and then dried over anhydrous magnesium sulfate. By removing the solvent by distillation under a reduced pressure, 978 mg of 1-phenylcyclopentanecarboxylic acid was obtained.