تفاعل #6663
ord-6d6b4bc9fa3d40c9a1bb0732d741e517
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1أخرى(equipped with a mechanical stirrer and a reflux condenser)
- 2درجة الحرارةthe mixture is heated
- 3درجة الحرارةat reflux for 3 hours
- 4درجة الحرارةThe reaction mixture is cooled down
- 5أخرىexcess ethyl iodide and the solvent are removed at reduced pressure on a rotary evaporator
- 6أخرىThe obtained dark tan-colored solids (162 gm) are further purified
- 7workup.DISSOLUTIONby dissolving in acetone (500 ml)
- 8أخرىfollowed by precipitation
- 9workup.ADDITIONby adding diethyl ether
- 10ترشيحFiltration
- 11أخرىair-drying the obtained solids
الإجراء التجريبي
1-[1-(4-chloro-phenyl)-cyclopropylmethyl]-1-ethyl-pyrrolidinium iodide is prepared from the reaction of the parent amine 1-[1-(4-chloro-phenyl)-cyclopropylmethyl]-pyrrolidine with ethyl iodide. A 100 gm (0.42 mole) of the amine, 1-[1-(4-chloro-phenyl)-cyclopropylmethyl]-pyrrolidine, is dissolved in 1000 ml anhydrous methanol in a 3-litre 3-necked reaction flask (equipped with a mechanical stirrer and a reflux condenser). To this solution, 98 gm (0.62 mole) of ethyl iodide is added, and the mixture is stirred at room temperature for 72 hours. Then, 39 gm (0.25 mol.) of ethyl iodide is added and the mixture is heated at reflux for 3 hours. The reaction mixture is cooled down and excess ethyl iodide and the solvent are removed at reduced pressure on a rotary evaporator. The obtained dark tan-colored solids (162 gm) are further purified by dissolving in acetone (500 ml) followed by precipitation by adding diethyl ether. Filtration and air-drying the obtained solids gives 153 gm (93% yield) of the desired 1-[1-(4-chloro-phenyl)-cyclopropylmethyl]-1-ethyl-pyrrolidinium iodide as a white powder. The product is pure by 1H and 13C-NMR analysis.