تفاعل #552538
ord-453cf5a3bf714af991360c2371dc7987
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرىas the reaction progresses
- 2غسيلthe mixture is washed twice with 20 ml of water each time
- 3تجفيفdried over sodium sulfate
- 4ترشيحfiltered
- 5أخرىthe solvent is evaporated
- 6أخرىis purified by column chromatography over silica gel (diethyl ether/toluene: 5/3)
- 7أخرىAfter the eluant mixture has been evaporated off
- 8أخرىto crystallise
- 9أخرىrecrystallised from diethyl ether/petroleum ether at 30°-50° C
- 10أخرىLight-brown crystals are obtained
- 11أخرىyield: 8.55 g (38 mmol) (=74.5% of the theoretical yield)
الإجراء التجريبي
10 g (51 mmol) of phenylguanidine hydrogen carbonate and 9.6 g (77 mmol) of 1-cyclopropyl-1,3-butanedione are heated at 110° C. for 6 hours with stirring the evolution of carbon dioxide which occurs subsiding as the reaction progresses. After the dark brown emulsion has been cooled to room temperature, 50 ml of diethyl ether are added and the mixture is washed twice with 20 ml of water each time, dried over sodium sulfate and filtered, and the solvent is evaporated. The dark brown oil which remains (=13.1 g) is purified by column chromatography over silica gel (diethyl ether/toluene: 5/3). After the eluant mixture has been evaporated off, the brown oil is made to crystallise and recrystallised from diethyl ether/petroleum ether at 30°-50° C. Light-brown crystals are obtained. Melting point: 67°-69° C.; yield: 8.55 g (38 mmol) (=74.5% of the theoretical yield).