تفاعل #1552025
ord-481194ab775a4ba3a016be36df738a48
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىobtained in the second step, in a reaction vessel
- 2أخرىequipped with a Dean-Stark apparatus under an atmosphere of nitrogen
- 3درجة الحرارةThe mixture was refluxed for 30 minutes
- 4أخرىwas removed with a Dean-Stark apparatus
- 5غسيلwas washed with water
- 6تجفيفThe solution was dried over anhydrous magnesium sulfate
- 7workup.DISTILLATIONthe solvent was distilled off under reduced pressure
- 8أخرىThe residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane=1/9 by volume)
الإجراء التجريبي
Toluene (50 ml) and p-toluenesulfonic acid monohydrate (0.14 g) were added to 3-butyl-1-(4-ethoxy-2,3-difluorophenyl)cyclopentanol (2.8 g) obtained in the second step, in a reaction vessel equipped with a Dean-Stark apparatus under an atmosphere of nitrogen. The mixture was refluxed for 30 minutes, while forming water was removed with a Dean-Stark apparatus. The reaction solution was cooled to room temperature and was washed with water. The solution was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane=1/9 by volume) to give a mixture (2.4 g) of 1-(3-butylcyclopent-1-enyl)-4-ethoxy-2,3-difluorobenzene and 1-(4-butylcyclopent-1-enyl)-4-ethoxy-2,3-difluorobenzene.