تفاعل #64929
ord-dfd625be54f44dbebb7c517ff09443f6
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1تركيزconcentrated
- 2workup.DISSOLUTIONThe residue is dissolved in 80 ml of ethyl acetate
- 3workup.ADDITION80 ml of petroleum ether are added
- 4workup.WAITThe mixture is left
- 5أخرىto crystallize out overnight
- 6ترشيحthe crystals (triphenylphosphine oxide and diethyl hydrazine-dicarboxylate) are filtered off
- 7تركيزThe filtrate is concentrated
- 8درجة الحرارةthe residue is heated
- 9درجة الحرارةunder reflux with 60 ml of concentrated hydrochloric acid overnight
- 10أخرىThe undissolved residues are decanted
- 11تركيزthe solution is concentrated
- 12استخلاصextracted five times with 50 ml of chloroform
- 13تجفيفThe extract is dried over potassium carbonate
- 14تركيزconcentrated
- 15workup.DISTILLATIONthe residue is distilled
الإجراء التجريبي
5.6 g (25 mmol) of trans-1-benzyl-3-hydroxy-4-methoxypyrrolidine and 8.6 g (33 mmol) of triphenylphosphine are initially introduced into 40 ml of absolute tetrahydrofuran and a solution of 6 g (34 mmol) of diethyl azodicarboxylate in 40 ml of absolute tetrahydrofuran is added dropwise at 0° C. 3.9 g (27 mmol) of phthalimide are then added in small portions at 0° C. in the course of one hour. The mixture is stirred at room temperature overnight and concentrated. The residue is dissolved in 80 ml of ethyl acetate and 80 ml of petroleum ether are added. The mixture is left to crystallize out overnight and the crystals (triphenylphosphine oxide and diethyl hydrazine-dicarboxylate) are filtered off. The filtrate is concentrated and the residue is heated under reflux with 60 ml of concentrated hydrochloric acid overnight. The undissolved residues are decanted and the solution is concentrated. The residue is taken up in a little water and the solution is rendered alkaline with solid potassium carbonate and extracted five times with 50 ml of chloroform. The extract is dried over potassium carbonate and concentrated and the residue is distilled.